Identity
- Trade Name
- C3 FDA UDI
- Generic Name
- Incontinence penis clamp, single-use FDA UDI
- Model / Reference
- Male Continence Device FDA UDI
Identifiers
- Catalog Number
- 910300 FDA UDI
- Primary DI / UDI-DI
- 08519520073347 FDA UDI
- FDA Product Code
- FHA FDA UDI
- GMDN Term
- Incontinence penis clamp, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5160 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Incontinence penis clamp, single-use
C3 by Personal Medical Corp. — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Personal Medical Corp.
Sources (1)
- FDA UDI 632763eb-8105-46b0-96bb-86a675c400ca 36 fields · synced May 30, 2026