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Conmed

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
CONMED MIXING AND DELIVERY KIT FDA UDI
Model / Reference
901201 FDA UDI
Description
CONMED MIXING AND DELIVERY KIT FDA UDI

Identifiers

Catalog Number
901201 FDA UDI
Primary DI / UDI-DI
10845854080658 FDA UDI
510(k) Number
K142535 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Arthroscopic surgical procedure kit, non-medicated, single-use

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

Similar devices

Also classified as Arthroscopic surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 5b7a0064-d852-43f7-bb07-8f85a9a9f8a4 37 fields · synced Jun 1, 2026