Ashish
October 14, 2026October 17, 2026
CDSCO, Compliance Guides, Import Compliance, Medical Devices

CDSCO Licence for Oxygen Masks & Nasal Cannula in India: Class A Registration and Process

Oxygen masks and nasal cannulae deliver supplemental oxygen from a source to the patient — simple, high-volume single-use accessories that are nonetheless regulated medical devices. CDSCO regulates oxygen masks and nasal cannulae as a Class A device with biocompatibility and oxygen-delivery performance behind the licence. This guide covers the full CDSCO pathway for oxygen masks and cannulae under the Medical Devices Rules, 2017 — classification, licence route, the standards, the documents, the fees and the timeline. This guide explains CDSCO registration for oxygen masks & nasal cannula in India — risk class, licence forms, standards, documents, fees and timeline.

Is a CDSCO Registration Mandatory for Oxygen Masks & Nasal Cannula?

Yes. An oxygen mask or nasal cannula is a notified Class A medical device and cannot be manufactured, imported or sold in India without a CDSCO licence. A domestic manufacturer holds a Form MD-5 licence from the State Licensing Authority. An importer holds a Form MD-15 import licence through an Indian Authorised Agent. Simple, Venturi, non-rebreather masks and nasal cannulae fall within the framework.

Risk Classification of Oxygen Masks & Nasal Cannula

Every medical device in India falls into one of four risk classes (A, B, C, D) under the First Schedule of the Medical Devices Rules, 2017. The class fixes the authority, the form, the fee, the audit route and the timeline.

Oxygen masks and nasal cannulae are classified as Class A (low risk). An oxygen mask/cannula is a low-risk, non-invasive, short-term device that delivers a medical gas externally, placing it in Class A under the First Schedule. Where a device could fall in two classes the higher class applies, and an accessory is classified in its own right. Always confirm against the current CDSCO classification list.

Which CDSCO Licence You Need for Oxygen Masks & Nasal Cannula

To manufacture oxygen masks & nasal cannulae in India (Class A) — apply in Form MD-3 to the State Licensing Authority (SLA); the licensing authority grants the licence in Form MD-5. A CDSCO-empanelled Notified Body audits the site. For Class A the audit is post-grant. For Class B the Notified Body conducts it before the licensing authority grants the licence.
To import oxygen masks & nasal cannulae (any class) — the overseas manufacturer appoints an Indian Authorised Agent who files Form MD-14 with the Central Licensing Authority; CDSCO grants the import licence in Form MD-15.
Test licence — for a small quantity imported or made for testing, evaluation, demonstration or clinical investigation: Form MD-12 application, Form MD-13 licence.
Loan licence — using another licensee’s approved premises: Form MD-4 (Class A/B) or Form MD-8 (Class C/D) for a licence in Form MD-6 or MD-10.

Applicable Standards for Oxygen Masks & Nasal Cannula

Oxygen masks and cannulae are evaluated on biocompatibility, connector and oxygen-delivery performance:

ISO 10993 series — biocompatibility of face/nose-contacting materials and the tubing.
Oxygen-delivery / FiO₂ performance across the flow range for the mask type.
Connector conformity for the oxygen-tubing connection.
ISO 11135 / 11137 — sterilisation validation where supplied sterile (many are supplied clean).
Flammability / oxygen-compatibility considerations for materials.
Shelf-life / stability data supporting the expiry.

Documents Required for CDSCO Registration of Oxygen Masks & Nasal Cannula

Whether you file for a manufacturing or an import licence, CDSCO expects the same core technical dossier built around the device:

Covering letter and application form — Form MD-3 (manufacture) or Form MD-14 (import) on the CDSCO Medical Device Online (SUGAM) portal, stating every device, variant and site.
Device Master File (DMF) — device description and intended use, materials, design and manufacturing information, ISO 14971 risk file, verification/validation data, sterilisation validation where applicable, shelf-life/stability data and the Essential Principles checklist.
Plant Master File (PMF) — site layout, equipment, utilities/HVAC, organisation chart with competent technical staff and the QMS procedures governing production.
ISO 13485 QMS certificate — current, with a scope covering the device.
Essential Principles of Safety and Performance — a completed checklist mapping the device against each applicable principle with the standard/evidence relied on.
Risk management file (ISO 14971) — hazards, risk controls and residual-risk justification.
Test / performance reports — against the applicable BIS/IS or ISO/IEC standards from an accredited laboratory.
Labels, IFU and packaging — meeting the labelling requirements of the Medical Devices Rules (manufacturer, licence number, sterile status, single-use symbols).
Undertaking and declaration of conformity to the Essential Principles and applicable standards.
Government fee receipt — paid online through the CDSCO portal.

Device-Specific Documents for Oxygen Masks & Nasal Cannula

Device-specific documents on top of the core set for oxygen masks & nasal cannulae:

Oxygen-delivery (FiO₂) performance data for the mask/cannula type across flows.
Biocompatibility (ISO 10993) for skin/mucosa-contacting parts.
Connector and tubing conformity evidence.
Sterility/cleanliness validation as applicable.
Shelf-life / stability data supporting the expiry.
Country-of-origin approval / Free Sale Certificate for imports.

For an import licence (Form MD-14) there are three further essentials:

Free Sale Certificate (FSC) — from the National Regulatory Authority of the country of origin, legalised (apostille/embassy attestation).
Country-of-origin regulatory approval — US FDA 510(k)/PMA, EU CE certificate or equivalent.
Power of Attorney and Authorised Agent licence — notarised, legalised PoA to the Indian Authorised Agent, plus the agent’s valid wholesale/manufacturing licence.

QMS & Essential Principles — What CDSCO Checks

Essential Principles of Safety and Performance (Fifth Schedule) — the device must be safe and perform as intended, with risks reduced as far as possible. Shown through recognised standards and the risk-management file.
Quality Management System (ISO 13485) — design controls, supplier control, process validation, traceability, complaint handling and CAPA, evidenced at audit.
Risk management (ISO 14971) — a living file with residual risks justified and communicated in the IFU.
Clinical evidence — proportionate to the class: clinical evaluation for lower-risk devices and clinical investigation data for many Class C/D and novel devices.

Label & IFU Requirements Specific to Oxygen Masks & Nasal Cannula

Oxygen-mask/cannula labelling is checked for type, size and single-use messaging:

Product type (simple/Venturi/non-rebreather mask, nasal cannula), size and tubing length.
Manufacturer name and address, and the CDSCO licence number.
Batch/lot number and date of manufacture (use-by date where sterile).
“Non-sterile” (or sterile with method) and a single-use symbol.
Flow-rate range/FiO₂ and oxygen-safety information in the IFU.

A Device, Not a Commodity

Because oxygen masks and cannulae are cheap and ubiquitous, they are sometimes treated as plastic commodities rather than medical devices — but they are Class A devices needing a CDSCO licence, with biocompatibility for skin/mucosa contact and oxygen-delivery evidence for the mask type. Venturi and non-rebreather masks make specific FiO₂ claims that must be supported. Register the range you supply and evidence the delivery performance and material safety.

Step-by-Step CDSCO Registration Process for Oxygen Masks & Nasal Cannula

Confirm the classification. Fix the risk class against the CDSCO classification list and the First Schedule — Class A here — which decides the form, authority, fee and audit route.
Choose the route. Manufacture (Form MD-3 → MD-5) or import (Form MD-14 → MD-15). Importers appoint an Indian Authorised Agent holding a valid manufacturing or wholesale licence.
Build the Device Master File and Plant Master File. Assemble device description, materials, design and process data, the ISO 14971 risk file, sterilisation/stability data and the site file with the QMS.
Complete the Essential Principles checklist. Map the device against each applicable essential principle and cite the BIS/IS or ISO/IEC standard or test report relied on.
Draw the test and performance reports. Test to the applicable standards at an accredited laboratory. Sterile and measuring devices carry additional validation.
Register and file on the CDSCO Online (SUGAM) portal. Create the account, pay the government fee online and upload the full dossier under the correct form.
Site audit / inspection. A CDSCO-empanelled Notified Body audits the site. For Class A the audit is post-grant. For Class B the Notified Body conducts it before the licensing authority grants the licence.
Respond to queries and receive the licence. Answer the deficiency letter within the stipulated period. On approval the licence issues in Form MD-5 (manufacture) or MD-15 (import).

CDSCO Registration Fees and Timeline for Oxygen Masks & Nasal Cannula

The Second Schedule of the Medical Devices Rules sets the fees, and you pay them online through the CDSCO portal. For manufacture of a Class A device the fee is Rs 5,000 per site plus Rs 500 for each distinct device, paid to the State Licensing Authority (SLA). CDSCO charges import fees under Form MD-15 per site and per device in USD — roughly USD 1,000 per site plus USD 50 per device for lower-risk devices, up to about USD 3,000 per site plus USD 1,500 per device for Class C and D. A test licence (Form MD-13) carries a modest fee. Always confirm the current figure on the CDSCO portal before filing.

A complete Class A manufacturing file typically clears in about three to six months. An import (MD-15) file usually takes six to nine months. Every deficiency letter effectively restarts the clock. Unlike the old registration certificates, an MDR 2017 licence does not expire — it stays valid as long as you pay the retention fee (equal to the licence fee) every five years and meet the conditions of licence.

Common Mistakes That Trigger a CDSCO Query

Common query reasons for oxygen-mask/cannula applications are:

FiO₂/oxygen-delivery claims (e.g. Venturi) not evidenced.
Biocompatibility missing for skin/mucosa-contacting parts.
Connector/tubing conformity not shown.
Sterility claim without validation.
Free Sale Certificate scope not covering all types/sizes on import.

Related Approvals to Plan Alongside CDSCO

DGFT Importer-Exporter Code — mandatory for any importer of record before the first consignment.
Wholesale / sale licence (Form 20B/21B or Form MD-42) — for stocking and distributing the device. The Indian Authorised Agent for an import licence must already hold one.
Legal Metrology (LMPC) registration — importers of pre-packaged devices declare MRP, net quantity, importer details and country of origin on the pack.
BIS certification — where the device or its electrical components fall under a mandatory BIS/CRS scheme.

Post-Approval Obligations

Print the licence number on the label and keep the Essential Principles conformity current.
Operate a Post-Market Surveillance (PMS) system and file the Periodic Safety Update Report (PSUR) on the schedule for the device’s class.
Report adverse events and field safety corrective actions through the Materiovigilance Programme of India (MvPI) and to CDSCO within the prescribed timelines.
Report any change in device, materials, site, labelling or QMS, and any regulatory action or recall in another country.
Retain distribution records for traceability and allow CDSCO to draw samples and inspect the premises.
Pay the retention fee every five years to keep the licence in force, and track BIS/ISO standard revisions.

FAQs on CDSCO Registration for Oxygen Masks & Nasal Cannula

What CDSCO class is an oxygen mask or nasal cannula?

Oxygen masks and nasal cannulae are Class A. A domestic manufacturer files Form MD-3 for an MD-5 licence. An importer files Form MD-14 for an MD-15 licence.

What evidence do oxygen masks need?

Biocompatibility (ISO 10993) for skin/mucosa-contacting parts and oxygen-delivery (FiO₂) performance for the mask type, plus connector conformity.

Are Venturi and non-rebreather masks different?

They make specific FiO₂ claims that must be supported by delivery-performance data, but they remain Class A oxygen-delivery devices.

Does a Class A device need a factory audit?

For Class A manufacture, the Notified Body audit is generally carried out after the MD-5 licence is granted, but the QMS and evidence must be in place at filing.

How long does registration take?

A complete Class A manufacturing (MD-5) file usually clears in about three to six months. An import (MD-15) file typically takes six to nine months.

Does the licence expire?

No — the MDR 2017 licence is perpetual, subject to the five-yearly retention fee and continued compliance.

Related CDSCO Registration Guides

Need end-to-end help? See our CDSCO registration services, or read these related guides:

Official references: Central Drugs Standard Control Organisation (CDSCO) and the CDSCO MD Online portal.

Why Choose PCN India Global

Classification triage — we confirm the correct risk class for your oxygen masks &amp. Nasal cannulae against the current CDSCO list before we draft anything.
Route selection — manufacture (MD-3/MD-5) or import (MD-14/MD-15), with the Indian Authorised Agent arrangement handled.
Dossier build — Device Master File, Plant Master File, Essential Principles checklist and ISO 13485/ISO 14971 readiness.
Standards and testing — the right BIS/IS or ISO/IEC standards mapped and accredited test reports coordinated.
End-to-end SUGAM filing — application, audit support, query response and the licence grant managed for you.
Adjacent approvals — DGFT/IEC, LMPC, wholesale/sale licence and BIS coordinated alongside your CDSCO licence.

PCN India Global manages the complete CDSCO process for oxygen masks &amp. Nasal cannulae — from classification and route selection to Device and Plant Master File preparation, SUGAM filing, audit support and the licence grant. WhatsApp or call +91 80109 05029, or email bdm@pcnindiaglobal.com, to get your registration underway.

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