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Lance Drill Ø1.5 x 3/5/7 mm
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 41152
by Neoss AB
Identity
- Trade Name
- Lance Drill Ø1.5 x 3/5/7 mm EUDAMEDNeoss Implant System FDA UDI
- Generic Name
- Fixture/appliance dental drill bit, single-use FDA UDI
- Device Name
- Single use Drill EUDAMEDLance Drill Ø1.5 x 3/5/7 mm FDA UDI
- Model / Reference
- 41152 EUDAMEDFDA UDI
- Description
- Lance Drill Ø1.5 x 3/5/7 mm FDA UDI
Identifiers
- Catalog Number
- 41152 FDA UDI
- Primary DI / UDI-DI
- 05060440331862 EUDAMEDFDA UDI
- Basic UDI-DI
- 506044033N0015MW EUDAMED
- Direct Marketing DI
- 05060440331862 EUDAMED
- FDA Product Code
- DZI FDA UDI
- EMDN Code
- P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
- GMDN Term
- Fixture/appliance dental drill bit, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 872.4120 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Lance Drill Ø1.5 x 3/5/7 mm by Neoss AB — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 506044033N0015MW | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Neoss AB
- EUDAMED SRN
- SE-MF-000022321
Sources (3)
- EUDAMED 9ba01bf5-1a03-4952-85ad-e1b6c4fae2e9 61 fields · synced Jun 18, 2026
- FDA UDI 24333de1-e3f9-4a3a-b848-9faaec53cf3c 35 fields · synced May 30, 2026
- EUDAMED b6e385b3-fd46-4140-9f67-1f77aa891b19 61 fields · synced Jun 18, 2026