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Conmed

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Endoscopic light source adaptor FDA UDI
Device Name
LIGHT GUIDE FITTING FOR A.C.M.I STYLE LIGHT SOURCES FDA UDI
Model / Reference
7455 FDA UDI
Description
LIGHT GUIDE FITTING FOR A.C.M.I STYLE LIGHT SOURCES FDA UDI

Identifiers

Catalog Number
7455 FDA UDI
Primary DI / UDI-DI
10845854038567 FDA UDI
510(k) Number
K850749 FDA UDI
FDA Product Code
KQM FDA UDI
GMDN Term
Endoscopic light source adaptor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscopic light source adaptor

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

Similar devices

Also classified as Endoscopic light source adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 745e8dbf-ffa5-49d2-906d-a71e966bab02 36 fields · synced Jun 6, 2026