Identity
- Trade Name
- Premier FDA UDI
- Generic Name
- Uterine tenaculum FDA UDI
- Device Name
- TENACULUM CERV ATRAU JAW 1/8 IN FDA UDI
- Model / Reference
- 9030611 FDA UDI
- Description
- TENACULUM CERV ATRAU JAW 1/8 IN FDA UDI
Identifiers
- Primary DI / UDI-DI
- D6919030611 FDA UDI
- FDA Product Code
- HDC FDA UDI
- GMDN Term
- Uterine tenaculum FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.4530 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Uterine tenaculum
Premier by Premier Dental Products Company — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Premier Dental Products Company
Sources (1)
- FDA UDI c60d68c1-160c-48ae-865f-6d5fe35894e2 33 fields · synced May 30, 2026