Identity
- Trade Name
- Implant Prosthetics FDA UDI
- Generic Name
- Root canal post, preformed FDA UDI
- Device Name
- NobelActive™/Conical-compatible 3.0mm Analog (10-Pack) FDA UDI
- Model / Reference
- 9004700-10 FDA UDI
- Description
- NobelActive™/Conical-compatible 3.0mm Analog (10-Pack) FDA UDI
Identifiers
- Catalog Number
- 9004700-10 FDA UDI
- Primary DI / UDI-DI
- 00842092124017 FDA UDI
- FDA Product Code
- EGG FDA UDI
- GMDN Term
- Root canal post, preformed FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3165 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
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
Implant Prosthetics by PREAT Corporation — 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
- PREAT Corporation
Sources (1)
- FDA UDI 09bd87d7-e924-42a7-bbbf-52a49f3dac7f 36 fields · synced Jun 8, 2026