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STOPCON Biopsy Valve For Pentax® GI-Endoscope

FDA UDI

Class II (US FDA UDI)

by GA Health Company Limited

Identity

Trade Name
STOPCON Biopsy Valve For Pentax® GI-Endoscope FDA UDI
Generic Name
Endoscope working-channel valve, single-use FDA UDI
Model / Reference
EN10234B FDA UDI

Identifiers

Primary DI / UDI-DI
04897106954100 FDA UDI
FDA Product Code
ODC FDA UDI
GMDN Term
Endoscope working-channel valve, 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope working-channel valve, single-use

STOPCON Biopsy Valve For Pentax® GI-Endoscope by GA Health Company Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope working-channel valve, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bf61959a-79de-4372-8783-56013ebd6537 32 fields · synced Jun 1, 2026