Identity
- Trade Name
- MEDENTiKA FDA UDI
- Generic Name
- Dental prosthesis removal instrument FDA UDI
- Device Name
- Abutment remover FDA UDI
- Model / Reference
- M 70 FDA UDI
- Description
- Abutment remover FDA UDI
Identifiers
- Catalog Number
- M 70 FDA UDI
- Primary DI / UDI-DI
- 04251574822949 FDA UDI
- FDA Product Code
- NDP FDA UDI
- GMDN Term
- Dental prosthesis removal instrument FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Commercial Distribution
- 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Conditional FDA UDI
Category: Dental prosthesis removal instrument
MEDENTiKA by Medentika GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental prosthesis removal instrument.
- HELMUT ZEPF — Helmut Zepf Medizintechnik GmbH · Class I
- devemed — devemed GmbH · Class I
- Karl Schumacher — KARL SCHUMACHER DENTAL, LLC · Class I
- ZOLL-DENTAL — Zoll-Dental · Class I
- STOMA® — Storz am Mark GmbH · Class I
- SCHWERT — A. Schweickhardt GmbH & Co. KG · Class I
- devemed — devemed GmbH · Class I
- STOMA® — Storz am Mark GmbH · Class I
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
- Medentika GmbH
Sources (1)
- FDA UDI 5d39aac4-deed-4ce1-ae42-fe84ecdd2051 35 fields · synced May 30, 2026