Identity
- Trade Name
- LATCH-TYPE EXTRACTOR FOR BROKEN SCREW FDA UDI
- Generic Name
- Dental implant extractor FDA UDI
- Model / Reference
- ETF FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08435389807810 FDA UDI
- FDA Product Code
- NDP FDA UDI
- GMDN Term
- Dental implant extractor 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
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: Dental implant extractor
Latch-Type Extractor For Broken Screw by Biotechnology Institute Sl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant extractor.
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- Explantation drill — Thommen Medical AG · Class I
- SIC invent Dental Implant Systems — SIC invent AG · Class I
- SwissPlus® — ZIMMER DENTAL INC. · Class I
- Explantation drill — Thommen Medical AG · 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
- Biotechnology Institute Sl
Sources (1)
- FDA UDI a105fff5-6db1-4408-951a-96134318ec88 32 fields · synced May 30, 2026