Identity
- Trade Name
- CediTEC DT EUDAMEDFDA UDI
- Generic Name
- Resin artificial teeth FDA UDI
- Device Name
- CediTEC DT EUDAMEDDisc A2 20 mm FDA UDI
- Model / Reference
- 6086 EUDAMEDFDA UDIDisc EUDAMED
- Description
- Disc A2 20 mm FDA UDI
Identifiers
- Catalog Number
- 6086 FDA UDI
- Primary DI / UDI-DI
- E22160861 EUDAMEDFDA UDI
- Basic UDI-DI
- B-E22160861 EUDAMED
- FDA Product Code
- ELM FDA UDI
- EMDN Code
- Q01020604 ORTHODONTIC DENTAL PROSTHESES EUDAMED
- GMDN Term
- Resin artificial teeth FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 872.3590 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
CediTEC DT by VOCO GmbH — Class II — FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- VOCO GmbH
Sources (2)
- FDA UDI 2fee067b-16f5-4db6-8a55-c81c19d3013a 36 fields · synced Oct 6, 2026
- EUDAMED ca4e94fb-971f-45ee-a4a2-701c46e5d7d3 61 fields · synced Jul 10, 2026