Identity
- Trade Name
- URETERO-RENO VIDEOSCOPE FDA UDI
- Generic Name
- Flexible video ureterorenoscope, reusable FDA UDI
- Model / Reference
- OLYMPUS URF-V3 FDA UDI
Identifiers
- Catalog Number
- N5782022 FDA UDI
- Primary DI / UDI-DI
- 04953170435119 FDA UDI
- 510(k) Number
- K181451 FDA UDI
- FDA Product Code
- FGB FDA UDI
- GMDN Term
- Flexible video ureterorenoscope, reusable 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Flexible video ureterorenoscope, reusable
Uretero-Reno Videoscope by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible video ureterorenoscope, reusable.
- COBRA VISION — Richard Wolf GmbH · Class II
- Flex-X — Karl Storz GmbH & Co. KG · Class II
- Flex-X — Karl Storz GmbH & Co. KG · Class II
- Flex-X — Karl Storz GmbH & Co. KG · Class II
- Flex-X / IMAGE 1 S — Karl Storz GmbH & Co. KG · Class II
- BOA VISION — Richard Wolf GmbH · Class II
- Flex-X — Karl Storz GmbH & Co. KG · Class II
- Flex-X / IMAGE 1 S — Karl Storz GmbH & Co. KG · Class II
Cleared under the same submission
K181451 also covers:
- URETERO-RENO FIBERSCOPE — Olympus Medical Systems Corporation
- URETERO-RENO FIBERSCOPE — Olympus Medical Systems Corporation
- URETERO-RENO FIBERSCOPE — Olympus Medical Systems Corporation
- URETERO-RENO FIBERSCOPE — Olympus Medical Systems Corporation
- URETERO-RENO VIDEOSCOPE — Olympus Medical Systems Corporation
- URETERO-RENO VIDEOSCOPE — Olympus Medical Systems Corporation
- URETERO-RENO VIDEOSCOPE — Olympus Medical Systems Corporation
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
- Olympus Medical Systems Corporation
Sources (1)
- FDA UDI 6e7f616d-de3b-4b51-ad10-3db494ab51b6 35 fields · synced Jun 8, 2026