Identity
- Trade Name
- Arthrex® FDA UDI
- Generic Name
- Rigid optical arthroscope, reusable FDA UDI
- Device Name
- ENDOSCOPE 70°,4x175.5MM,HD,REV LGHT POST FDA UDI
- Model / Reference
- AR-3070AWR FDA UDI
- Description
- ENDOSCOPE 70°,4x175.5MM,HD,REV LGHT POST FDA UDI
Identifiers
- Catalog Number
- AR-3070AWR FDA UDI
- Primary DI / UDI-DI
- 00888867194618 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Rigid optical arthroscope, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Rigid optical arthroscope, reusable
Arthrex® by Arthrex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid optical arthroscope, reusable.
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- HOPKINS — Karl Storz GmbH & Co. KG · Class II
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- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- HOPKINS — Karl Storz GmbH & Co. KG · Class II
- Precision Ideal Eyes — Stryker Corp. · Class II
- HNM MEDICAL — HNM STAINLESS, LLC. · Class I
- AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, 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 |
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Manufacturer
- Manufacturer
- Arthrex, Inc.
Sources (1)
- FDA UDI 598d3667-1832-423a-8e32-2b9a1517a101 35 fields · synced May 30, 2026