Identity
- Trade Name
- ADITEK FDA UDI
- Generic Name
- Orthodontic wire FDA UDI
- Device Name
- Archwire Sequence Contour Niti 35° EasyClip+ Passive 14/18/14X25/17X25/ w/8 FDA UDI
- Model / Reference
- 09.08.9002 FDA UDI
- Description
- Archwire Sequence Contour Niti 35° EasyClip+ Passive 14/18/14X25/17X25/ w/8 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07899439254695 FDA UDI
- GMDN Term
- Orthodontic wire FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Category: Orthodontic wire
Aditek by Aditek Do Brasil S/A — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- ORTHOSOURCE — Ortho Source · Class I
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Aditek Do Brasil S/A
Sources (1)
- FDA UDI d14f94ec-160e-4bcf-991a-39691b2de839 33 fields · synced Jun 8, 2026