Identity
- Trade Name
- Arthrorazor FDA UDI
- Generic Name
- Arthroscopic shaver system blade, single-use FDA UDI
- Model / Reference
- 2077.01424 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860012754878 FDA UDI
- FDA Product Code
- GFA FDA UDI
- GMDN Term
- Arthroscopic shaver system blade, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Arthroscopic shaver system blade, single-use
Arthrorazor by Orthodoxo LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Arthroscopic shaver system blade, single-use.
- DYONICS / SYNOVATOR — Smith & Nephew, Inc. · Class I
- SharkCut — Techcord co., Ltd · Class I
- SharkCut — Techcord co., Ltd · Class I
- Arthrex® — Arthrex, Inc. · Class I
- FMS — Medos International Sàrl · Class II
- STERLING — Conmed Corporation · Class I
- VOLMED BRASIL — VOLMED BRASIL EQUIPAMENTOS LTDA · Class I
- SharkCut — Techcord co., Ltd · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Orthodoxo LLC
Sources (1)
- FDA UDI 37fedeee-bb97-4cec-8e0b-4937025697ad 32 fields · synced May 30, 2026