← Back to catalogue
Ss Archwire Universal L 016 W/10
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 09.05.0916Model Archwires and Wires
Identity
- Trade Name
- SS ARCHWIRE UNIVERSAL L 016 W/10 EUDAMEDADITEK FDA UDI
- Generic Name
- Orthodontic wire FDA UDI
- Device Name
- SS Archwire Universal L 016 w/10 EUDAMEDFDA UDI
- Model / Reference
- Archwires and Wires EUDAMED09.05.0916 EUDAMEDFDA UDI
- Description
- SS Archwire Universal L 016 w/10 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07899439209602 EUDAMEDFDA UDI
- Basic UDI-DI
- 7899439209JC EUDAMEDB-07899439209602 EUDAMED
- FDA Product Code
- DZC FDA UDI
- EMDN Code
- Q010405 ORTHODONTIC WIRES EUDAMED
- GMDN Term
- Orthodontic wire FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.5410 FDA UDI
- Market of Registration
- Spain 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
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
No
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
Yes
FDA UDI
Ss Archwire Universal L 016 W/10 by Aditek do Brasil SA — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 7899439209JC | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 7899439209JC | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aditek do Brasil SA
- EUDAMED SRN
- BR-MF-000018793
- Authorised Representative
- EC Certification Service GmbH AT-AR-000006658
Sources (3)
- EUDAMED 9265a1ea-9063-436f-8073-4e8c7fd3d0a7 61 fields · synced Jul 12, 2026
- FDA UDI f89a806d-2b21-4de7-b88d-3e65c9162bc4 33 fields · synced May 30, 2026
- EUDAMED b15264af-db14-4171-973b-a5c190500b47 61 fields · synced Jun 19, 2026