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Conmed

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Sternum saw blade, single-use FDA UDI
Device Name
REPEAT STERNOTOMY BLADE, 44.5 X 40 X 0.4 MM (.016") FDA UDI
Model / Reference
00507122800 FDA UDI
Description
REPEAT STERNOTOMY BLADE, 44.5 X 40 X 0.4 MM (.016") FDA UDI

Identifiers

Catalog Number
5071-228 FDA UDI
Primary DI / UDI-DI
10845854005002 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Sternum saw blade, 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
Height — 0.4 Millimeter FDA UDI
Width — 40 Millimeter FDA UDI
Height — 0.016 Inch FDA UDI
Length — 44.5 Millimeter FDA UDI

Category: Sternum saw blade, single-use

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

Similar devices

Also classified as Sternum saw blade, 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 cbf1edd9-8b14-4e43-805b-d85e43083462 36 fields · synced May 30, 2026