Protection Analog / Drill Guide CC RP 5/pkg
EUDAMEDFDA UDIClass I (EU MDR)
Identity
- Trade Name
- Protection Analog / Drill Guide CC RP 5/pkg EUDAMEDNA FDA UDI
- Generic Name
- Dental implant suprastructure, temporary, preformed, reusable FDA UDI
- Device Name
- Reusable lab tools for prosthetics EUDAMEDProtection Analog / Drill Guide CC RP 5/pkg FDA UDI
- Model / Reference
- 38856 EUDAMEDFDA UDI
- Description
- Protection Analog / Drill Guide CC RP 5/pkg FDA UDI
Identifiers
- Catalog Number
- 38856 FDA UDI
- Primary DI / UDI-DI
- 07332747213188 EUDAMEDFDA UDI
- Basic UDI-DI
- 73327470000002026Q EUDAMED
- Unit of Use DI
- 07332747155020 EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY 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
Single Use
No
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Dimensions & Sizes
- Size
- Outer Diameter — 5.200 Millimeter FDA UDILength — 15.000 Millimeter FDA UDI
Category: Dental implant suprastructure, temporary, preformed, single-use
Get the most accurate and up-to-date information about the Protection Analog / Drill Guide CC RP 5/pkg medical device. This device is designed for reusable lab tools for prosthetics, offering a comprehensive set of features that make it an essential tool in various healthcare settings.
Similar devices
Also classified as Dental implant suprastructure, temporary, preformed, single-use.
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- Scanbody Screw — ARUM DENTISTRY Co., Ltd. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
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 |
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Manufacturer
- Manufacturer
- Nobel Biocare AB
- EUDAMED SRN
- SE-MF-000000009
Sources (2)
- EUDAMED 41cdfede-7368-44a2-b5ad-2cb78aadebb5 61 fields · synced Jul 9, 2026
- FDA UDI da5b00c4-499d-4587-bd8a-e855ec6226ae 37 fields · synced May 30, 2026