Identity
- Trade Name
- BioDerm (Men's Liberty Acute) FDA UDI
- Generic Name
- Urinary incontinence penis sheath/port, single-use FDA UDI
- Device Name
- BioDerm Men's Liberty Acute for iMEDicare FDA UDI
- Model / Reference
- 20026-10 FDA UDI
- Description
- BioDerm Men's Liberty Acute for iMEDicare FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00653599000816 FDA UDI
- FDA Product Code
- NOA FDA UDI
- GMDN Term
- Urinary incontinence penis sheath/port, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5250 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Category: Urinary incontinence penis sheath/port, single-use
BioDerm (Men's Liberty Acute) by Argentum Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Argentum Medical, Llc
Sources (1)
- FDA UDI 1a10fcd5-3cb6-407a-8bc5-325daeb9d664 35 fields · synced May 31, 2026