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Edge

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Edge FDA UDI
Generic Name
Endoscope working-channel valve, single-use FDA UDI
Device Name
Bronchoscope Adapter;For use with Fujinon bronchoscopes FDA UDI
Model / Reference
SD302BAPK FDA UDI
Description
Bronchoscope Adapter;For use with Fujinon bronchoscopes FDA UDI

Identifiers

Primary DI / UDI-DI
10884521539761 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
Endoscope working-channel valve, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 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

Yes

FDA UDI

Category: Endoscope working-channel valve, single-use

Edge by Covidien LP — 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

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI ee87c25a-a9a3-4f72-ba67-13f109cd02f9 35 fields · synced May 30, 2026