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Uro-G Flexible Cystoscope

FDA UDI

Class II (US FDA UDI)

by UroViu Corporation

Identity

Trade Name
Uro-G Flexible Cystoscope FDA UDI
Generic Name
Flexible video cystoscope, single-use FDA UDI
Device Name
The Uro-G Flexible Cystoscope System consists of a multi-use handle with an LCD screen and a single-use sterile cannula. The Uro-G Flexible Cystoscope is intended for endoscopic diagnosis and infusion of irrigating fluid within the bladder and urethra. FDA UDI
Model / Reference
1520 FDA UDI
Description
The Uro-G Flexible Cystoscope System consists of a multi-use handle with an LCD screen and a single-use sterile cannula. The Uro-G Flexible Cystoscope is intended for endoscopic diagnosis and infusion of irrigating fluid within the bladder and urethra. FDA UDI

Identifiers

Catalog Number
1520 FDA UDI
Primary DI / UDI-DI
00860008483706 FDA UDI
510(k) Number
K202921 FDA UDI
FDA Product Code
FAJ FDA UDI
GMDN Term
Flexible video cystoscope, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Flexible video cystoscope, single-use

Uro-G Flexible Cystoscope by UroViu Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video cystoscope, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
UroViu Corporation

Sources (1)

  • FDA UDI 1910a91f-cc07-46da-9a47-3e3913566011 37 fields · synced May 31, 2026