Identity
- Trade Name
- Timm Medical FDA UDI
- Generic Name
- Penile vacuum device FDA UDI
- Model / Reference
- Osbon ErecAid Classic International FDA UDI
Identifiers
- Catalog Number
- XX02 FDA UDI
- Primary DI / UDI-DI
- 00857312008114 FDA UDI
- GMDN Term
- Penile vacuum device FDA UDI
Classification
- 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
No
FDA UDI
Over-the-Counter
Yes
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Penile vacuum device
Timm Medical by Pos-T-Vac LLC — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Pos-T-Vac LLC
Sources (1)
- FDA UDI 93d5d6ea-255a-455b-9142-b779a2545734 33 fields · synced Jun 8, 2026