Identity
- Trade Name
- CONMED FDA UDI
- Generic Name
- Rigid optical arthroscope, reusable FDA UDI
- Device Name
- 4MM, 30 DEGREE HD QUICKLATCH AUTOCLAVABLE EYECUP SCOPE FDA UDI
- Model / Reference
- HD4300 FDA UDI
- Description
- 4MM, 30 DEGREE HD QUICKLATCH AUTOCLAVABLE EYECUP SCOPE FDA UDI
Identifiers
- Catalog Number
- HD4300 FDA UDI
- Primary DI / UDI-DI
- 20845854027100 FDA UDI
- 510(k) Number
- K962075 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
- Not 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Angle — 30 degree FDA UDIOuter Diameter — 4 Millimeter FDA UDI
Conmed by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Conmed Corporation
Sources (1)
- FDA UDI 5c5f9656-22fe-4098-a4b8-4a47bebef664 39 fields · synced May 31, 2026