Identity
- Trade Name
- SCHEU-Anchor FDA UDI
- Generic Name
- Orthodontic wire FDA UDI
- Device Name
- SCHEU-Anchor Ø 0.8 mm FDA UDI
- Model / Reference
- 2050.3 FDA UDI
- Description
- SCHEU-Anchor Ø 0.8 mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- J01820503 FDA UDI
- FDA Product Code
- EHP FDA UDI
- GMDN Term
- Orthodontic wire FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3285 FDA UDI
- 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
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
No
FDA UDI
Category: Orthodontic wire
SCHEU-Anchor by Scheu-Dental — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthodontic wire.
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- Reflex Nickel Titanium Wire — TP ORTHODONTICS, INC. · Class I
- Pg Supply — Pg Supply, Inc. · Class I
- 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 | Class I | Pending data |
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Manufacturer
- Manufacturer
- Scheu-Dental
Sources (1)
- FDA UDI 0d2f7b78-c7dc-4829-829a-04716aa1ba82 33 fields · synced Jun 1, 2026