Identity
- Trade Name
- S9 FDA UDI
- Generic Name
- Home BPAP unit FDA UDI
- Device Name
- S9 VPAP Adapt FDA UDI
- Model / Reference
- 36377 FDA UDI
- Description
- S9 VPAP Adapt FDA UDI
Identifiers
- Catalog Number
- 36377 FDA UDI
- Primary DI / UDI-DI
- 00619498363773 FDA UDI
- FDA Product Code
- BZD FDA UDI
- GMDN Term
- Home BPAP unit 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Home BPAP unit
S9 by Resmed Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Home BPAP unit.
- Air Filter — Bmc Medical., Ltd. · Class II
- BiPAP System One 60 Series — Respironics, Inc. · Class II
- DreamStation — Respironics, Inc. · Class II
- BiPAP System One 60 Series — Respironics, Inc. · Class II
- VPAP — Resmed Corp · Class II
- DreamStation — Respironics, Inc. · Class II
- BiPAP System One 60 Series — Respironics, Inc. · Class II
- DreamStation — Respironics, 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 Pty Ltd
Sources (1)
- FDA UDI 396d67f1-8682-4cf9-b226-ebf547b4745e 35 fields · synced Jun 1, 2026