Identity
- Trade Name
- ORTHO ARCH FDA UDI
- Generic Name
- Orthodontic archwire FDA UDI
- Device Name
- .021 X .025 RIGHT FORM KEYHOLE 4-LOOP 36MM (10)***DISCONTINUED/ WHILE SUPPLIES LAST. NON-REFUNDABLE OR RETURNABLE*** FDA UDI
- Model / Reference
- .021 X .025 RIGHT FORM 4-LOOP 36MM FDA UDI
- Description
- .021 X .025 RIGHT FORM KEYHOLE 4-LOOP 36MM (10)***DISCONTINUED/ WHILE SUPPLIES LAST. NON-REFUNDABLE OR RETURNABLE*** FDA UDI
Identifiers
- Catalog Number
- 105-036 FDA UDI
- Primary DI / UDI-DI
- D90910503612 FDA UDI
- FDA Product Code
- DZC FDA UDI
- GMDN Term
- Orthodontic archwire FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.5410 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 archwire
Ortho Arch by Ortho Arch Company Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Ortho Arch Company Inc
Sources (1)
- FDA UDI 0298d6ae-f783-41a2-b5cc-f6037203512e 34 fields · synced May 30, 2026