← Back to catalogue
Lab Screw Implant Level CC RP/WP and Ext Hex RP 5/pkg
EUDAMEDFDA UDIClass I (EU MDR)
Ref 37895
Identity
- Trade Name
- Lab Screw Implant Level CC RP/WP and Ext Hex RP 5/pkg EUDAMEDNobel Biocare® FDA UDI
- Generic Name
- Dental implant suprastructure, temporary, preformed, reusable FDA UDI
- Device Name
- Reusable lab tools for prosthetics EUDAMEDLab Screw Implant Level CC RP/WP and Ext Hex RP 5/pkg FDA UDI
- Model / Reference
- 37895 EUDAMEDFDA UDI
- Description
- Lab Screw Implant Level CC RP/WP and Ext Hex RP 5/pkg FDA UDI
Identifiers
- Catalog Number
- 37895 FDA UDI
- Primary DI / UDI-DI
- 07332747212303 EUDAMEDFDA UDI
- Basic UDI-DI
- 73327470000002026Q EUDAMED
- Unit of Use DI
- 07332747150292 EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- Q010299 PROSTHETIC DENTISTRY DEVICES - OTHER EUDAMED
- GMDN Term
- Dental implant suprastructure, temporary, preformed, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Market of Registration
- Sweden EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Lab Screw Implant Level CC RP/WP and Ext Hex RP 5/pkg by Nobel Biocare AB — Class I — 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 | 73327470000002026Q | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Nobel Biocare AB
- EUDAMED SRN
- SE-MF-000000009
Sources (2)
- EUDAMED 3475a8d3-b99b-4727-bae3-2e9909870d4e 61 fields · synced Jun 19, 2026
- FDA UDI 74480d97-1c6e-49a9-849e-bafa3f96dc6e 36 fields · synced May 30, 2026