Identity
- Trade Name
- DeVilbiss FDA UDI
- Generic Name
- Home CPAP unit FDA UDI
- Device Name
- Part Sleep Flow Generator Accessories Product Description CONTROL BOARD FDA UDI
- Model / Reference
- DV55D-673 FDA UDI
- Description
- Part Sleep Flow Generator Accessories Product Description CONTROL BOARD FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00885304006749 FDA UDI
- FDA Product Code
- BZD FDA UDI
- GMDN Term
- Home CPAP unit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5905 FDA UDI
- Commercial Distribution
- Not 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
DeVilbiss by Drive Devilbiss Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Drive Devilbiss Healthcare
Sources (1)
- FDA UDI 0b7f380d-c1b2-4a95-b1f3-b6def2da6e3d 34 fields · synced Jun 8, 2026