Identity
- Trade Name
- ASP MEDICAL FDA UDI
- Generic Name
- Hand-held urinal, single-use FDA UDI
- Device Name
- URINAL, MALE, 32 OZ, NON-STERILE FDA UDI
- Model / Reference
- MRT132 FDA UDI
- Description
- URINAL, MALE, 32 OZ, NON-STERILE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840216103696 FDA UDI
- FDA Product Code
- FNP FDA UDI
- GMDN Term
- Hand-held urinal, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6730 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
Yes
FDA UDI
Prescription Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Asp Medical by Asp Global, 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
- Asp Global, LLC
Sources (1)
- FDA UDI a9ee11e6-b238-4114-bc60-8925a865e1ad 34 fields · synced Jun 1, 2026