Identity
- Trade Name
- Arthrex® FDA UDI
- Generic Name
- Rigid optical arthroscope, single-use FDA UDI
- Device Name
- NANONEEDLE SCOPE, 180MM FDA UDI
- Model / Reference
- AR-3210-0044 FDA UDI
- Description
- NANONEEDLE SCOPE, 180MM FDA UDI
Identifiers
- Catalog Number
- AR-3210-0044 FDA UDI
- Primary DI / UDI-DI
- 00888867375567 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Rigid optical arthroscope, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Rigid optical arthroscope, single-use
Arthrex® by Arthrex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid optical arthroscope, single-use.
- CIT Ortho — Cit Ortho · Class II
- AccessVu 90 — INTRAVU, INC. · Class II
- mi-eye 3 — TRICE MEDICAL, INC. · Class II
- Prosurg — Prosurg, Inc · Class II
- CIT Ortho — Cit Ortho · Class II
- AccessVu 60 — INTRAVU, INC. · Class II
- CIT Ortho — Cit Ortho · Class II
- Prosurg — Prosurg, Inc · Class II
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Arthrex, Inc.
Sources (1)
- FDA UDI c62c6b8d-a103-44a0-984e-d508be8d2340 35 fields · synced Jun 1, 2026