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CleanGuard

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CleanGuard FDA UDI
Generic Name
Endoscope channel support kit FDA UDI
Device Name
CleanGuard Disposable Endoscope Valves Set, Contains Air/Water Valve, Suction Valve and Biopsy Valve FDA UDI
Model / Reference
200305 FDA UDI
Description
CleanGuard Disposable Endoscope Valves Set, Contains Air/Water Valve, Suction Valve and Biopsy Valve FDA UDI

Identifiers

Catalog Number
200305 FDA UDI
Primary DI / UDI-DI
20653405986475 FDA UDI
FDA Product Code
OCX FDA UDI
GMDN Term
Endoscope channel support kit 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope channel support kit

CleanGuard by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope channel support kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 3fae2b66-6c0b-4de3-97df-3e71c0a1fcb8 36 fields · synced Jun 8, 2026