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Conmed

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Medical device integration rack FDA UDI
Device Name
VISUALIZATION CART, 120 VAC FDA UDI
Model / Reference
AV8500 FDA UDI
Description
VISUALIZATION CART, 120 VAC FDA UDI

Identifiers

Catalog Number
AV8500 FDA UDI
Primary DI / UDI-DI
30845854050723 FDA UDI
FDA Product Code
KQM FDA UDI
GMDN Term
Medical device integration rack 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical device integration rack

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

Similar devices

Also classified as Medical device integration rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI aa39c88b-bb22-4cb3-bcbc-e6c45cd37ea8 36 fields · synced Jun 6, 2026