Identity
- Trade Name
- BOEHRINGER® CareDry™ Porifem FDA UDI
- Generic Name
- Female wearable urinal, single-use FDA UDI
- Device Name
- CareDry™ Sponge FDA UDI
- Model / Reference
- 7645 FDA UDI
- Description
- CareDry™ Sponge FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10816286021045 FDA UDI
- FDA Product Code
- NZU FDA UDI
- GMDN Term
- Female wearable urinal, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5250 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
BOEHRINGER® CareDry™ Porifem by Boehringer Laboratories, Llc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Boehringer Laboratories, Llc
Sources (1)
- FDA UDI 5e40ff68-b8a6-4f5e-b98f-9ba54a8ff7d3 35 fields · synced Jun 8, 2026