Identity
- Trade Name
- Nephroscope FDA UDI
- Generic Name
- Rigid optical nephroscope FDA UDI
- Model / Reference
- 165 800 002BC001 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04059082004242 FDA UDI
- 510(k) Number
- K945262 FDA UDI
- FDA Product Code
- FAJ FDA UDI
- GMDN Term
- Rigid optical nephroscope 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
No
FDA UDI
Single Use
No
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
No
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: Rigid optical nephroscope
Nephroscope by SOPRO-COMEG GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid optical nephroscope.
- PANOVIEW PLUS — Richard Wolf GmbH · Class II
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class II
- Olympus — Olympus Winter & Ibe GmbH · Class II
- PANOVIEW — Richard Wolf GmbH · Class II
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class II
- PANOVIEW — Richard Wolf GmbH · Class II
- Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class II
- PANOVIEW PLUS — Richard Wolf GmbH · Class II
Cleared under the same submission
K945262 also covers:
- Accessory for urology — SOPRO-COMEG GmbH
- Accessory for urology — SOPRO-COMEG GmbH
- Accessory for urology — SOPRO-COMEG GmbH
- Accessory for urology — SOPRO-COMEG GmbH
- Accessory for urology — SOPRO-COMEG GmbH
- Accessory for urology — SOPRO-COMEG GmbH
- Accessory for urology — SOPRO-COMEG GmbH
- Accessory for urology — SOPRO-COMEG GmbH
- Adaptor — SOPRO-COMEG GmbH
- Cystoscope — SOPRO-COMEG GmbH
- Cystoscope — SOPRO-COMEG GmbH
- Cystoscope — SOPRO-COMEG GmbH
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
- SOPRO-COMEG GmbH
Sources (1)
- FDA UDI ab363d1e-6579-49b9-9469-33ebff3da6bd 33 fields · synced May 30, 2026