Identity
- Trade Name
- MIRAGE FFM FDA UDI
- Generic Name
- CPAP/BPAP face mask, reusable FDA UDI
- Device Name
- MIRAGE FFM SER 2 CUSH MED-SHLW FDA UDI
- Model / Reference
- 16672 FDA UDI
- Description
- MIRAGE FFM SER 2 CUSH MED-SHLW FDA UDI
Identifiers
- Catalog Number
- 16672 FDA UDI
- Primary DI / UDI-DI
- 00619498166725 FDA UDI
- FDA Product Code
- BZD FDA UDI
- GMDN Term
- CPAP/BPAP face mask, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5905 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: CPAP/BPAP face mask, reusable
Mirage Ffm by Resmed Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as CPAP/BPAP face mask, reusable.
- AMARA — Respironics, Inc. · Class II
- AIRFIT F20 — RESMED PTY LTD · Class II
- AIRFIT F20 NON MAGNETIC — RESMED PTY LTD · Class II
- PERFORMAX — Respironics, Inc. · Class II
- HOSPITAL FFM — RESMED PTY LTD · Class II
- Amara View — Respironics, Inc. · Class II
- QUATTRO FX — RESMED PTY LTD · Class II
- Full Face CPAP Mask — Large — SUNSET HEALTHCARE SOLUTIONS, Inc. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Resmed Corp
Sources (1)
- FDA UDI 74a19db5-f6b0-448f-8adf-9325ad18e025 36 fields · synced Jun 8, 2026