Identity
- Trade Name
- MABIS DMI FDA UDI
- Generic Name
- Surgical penis clamp, single-use FDA UDI
- Device Name
- PLASTIBELL HOSPITAL BULK 1.2CM FDA UDI
- Model / Reference
- D 9212 FDA UDI
- Description
- PLASTIBELL HOSPITAL BULK 1.2CM FDA UDI
Identifiers
- Catalog Number
- D 9212 FDA UDI
- Primary DI / UDI-DI
- 10767056092126 FDA UDI
- FDA Product Code
- FHG FDA UDI
- GMDN Term
- Surgical penis clamp, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.4530 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
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
Mabis Dmi by Dms Holdings, Inc., — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Dms Holdings, Inc.,
Sources (1)
- FDA UDI 3aa604da-40a7-4705-8ccd-81406d435287 35 fields · synced Jun 1, 2026