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Conmed

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Orthopaedic bur, single-use FDA UDI
Device Name
ROUND BUR, CARBIDE, 1.0MM FDA UDI
Model / Reference
00509322000 FDA UDI
Description
ROUND BUR, CARBIDE, 1.0MM FDA UDI

Identifiers

Catalog Number
5093-220 FDA UDI
Primary DI / UDI-DI
10845854003329 FDA UDI
FDA Product Code
GFF FDA UDI
GMDN Term
Orthopaedic bur, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 1 Millimeter FDA UDI

Category: Orthopaedic bur, single-use

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

Similar devices

Also classified as Orthopaedic bur, 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 7344dc03-c82f-422c-8909-507d7884a38c 36 fields · synced May 31, 2026