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Neoss Implant System
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref 41120
by Neoss, Ltd.
Identity
- Trade Name
- Drill Extender EUDAMEDNeoss Implant System FDA UDI
- Generic Name
- Dental drill bit extension FDA UDI
- Device Name
- Handpiece connection instrument EUDAMEDDrill Extender FDA UDI
- Model / Reference
- 41120 EUDAMEDFDA UDI
- Description
- Drill Extender FDA UDI
Identifiers
- Catalog Number
- 41120 FDA UDI
- Primary DI / UDI-DI
- 05060440331725 EUDAMEDFDA UDI
- Basic UDI-DI
- 506044033N0035N4 EUDAMED
- Direct Marketing DI
- 05060440331725 EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
- GMDN Term
- Dental drill bit extension FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental drill bit extension
Neoss Implant System by Neoss, Ltd. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Dental drill bit extension.
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Neoss, Ltd.
Sources (2)
- FDA UDI 7ef5ecb8-c25d-4774-bb28-17e1b690b9e1 35 fields · synced Sep 17, 2026
- EUDAMED 3750aa1c-a2e7-42ad-b7c8-6f1163cc97e2 61 fields · synced Sep 17, 2026