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RenaNav Video Processing Unit

FDA UDI

Class II (US FDA UDI)

by CenterPoint Systems LLC

Identity

Trade Name
RenaNav Video Processing Unit FDA UDI
Generic Name
Endoscopic video image processing unit FDA UDI
Device Name
Video processing unit for RenaNav Single-Use Digital Flexible Ureteroscope FDA UDI
Model / Reference
NVS-MD-000386 FDA UDI
Description
Video processing unit for RenaNav Single-Use Digital Flexible Ureteroscope FDA UDI

Identifiers

Primary DI / UDI-DI
00810024670376 FDA UDI
510(k) Number
K223097 FDA UDI
FDA Product Code
FGB FDA UDI
GMDN Term
Endoscopic video image processing unit 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic video image processing unit

RenaNav Video Processing Unit by CenterPoint Systems LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing unit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d1cd07fa-8e4e-4dd2-ac49-451aeb34503a 34 fields · synced Jun 9, 2026