Identity
- Trade Name
- Protemp™ II FDA UDI
- Generic Name
- Temporary dental crown/bridge FDA UDI
- Device Name
- 3M™ ESPE™ Protemp™ II Composite For Temporary Crowns And Bridges Refill A3 Light, 46100 FDA UDI
- Model / Reference
- 46100 FDA UDI
- Description
- 3M™ ESPE™ Protemp™ II Composite For Temporary Crowns And Bridges Refill A3 Light, 46100 FDA UDI
Identifiers
- Catalog Number
- 46100 FDA UDI
- Primary DI / UDI-DI
- J001702011132330 FDA UDI
- FDA Product Code
- EID FDA UDIEBG FDA UDI
- GMDN Term
- Temporary dental crown/bridge FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI872.3770 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Temporary dental crown/bridgeDental material cartridge-plunging applicator, two-component, manual
Protemp™ II by 3M Deutschland GmbH — 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
- 3M Deutschland GmbH
Sources (1)
- FDA UDI 9456d1f1-8c33-4465-9f68-c226587647bc 35 fields · synced Jun 8, 2026