Identity
- Trade Name
- Arthrex® FDA UDI
- Generic Name
- Implantable bone nut FDA UDI
- Device Name
- NUT, PIN FIXATION, FOR AR-1399 DRIVER FDA UDI
- Model / Reference
- AR-1890 FDA UDI
- Description
- NUT, PIN FIXATION, FOR AR-1399 DRIVER FDA UDI
Identifiers
- Catalog Number
- AR-1890 FDA UDI
- Primary DI / UDI-DI
- 00888867022416 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Implantable bone nut FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Implantable bone nut
Arthrex® by Arthrex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Implantable bone nut.
- HOFFMANN — Stryker Corp. · Class II
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- T2 — Stryker Corp. · Class I
- Nut — I.T.S. GmbH · Class II
- Medline — MEDLINE INDUSTRIES, INC. · Class II
- M/DN® — Zimmer, Inc. · Class II
- AXSOS — Stryker Corp. · 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
- Arthrex, Inc.
Sources (1)
- FDA UDI 3bb76d90-a3fa-412b-b1ed-8a78fa022fb3 35 fields · synced May 30, 2026