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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
SMALL JOINT ELECTRODE BASIC KIT; 90 DEGREE TIP FDA UDI
Model / Reference
8323BA FDA UDI
Description
SMALL JOINT ELECTRODE BASIC KIT; 90 DEGREE TIP FDA UDI

Identifiers

Catalog Number
8323BA FDA UDI
Primary DI / UDI-DI
20845854013271 FDA UDI
510(k) Number
K823424 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Commercial Distribution
Not 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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Angle — 90 degree FDA UDI

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

Cleared under the same submission

K823424 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI bc0fab7e-165a-4863-9e54-e1e7e9768f37 38 fields · synced May 30, 2026