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Me-92

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
ME-92 FDA UDI
Generic Name
Surgical saw blade, oscillating, single-use FDA UDI
Device Name
OSCILLATOR BLADE, ME-92 COATED ,25.4 X 80 X 1.2 MM (.047") FDA UDI
Model / Reference
00507114000 FDA UDI
Description
OSCILLATOR BLADE, ME-92 COATED ,25.4 X 80 X 1.2 MM (.047") FDA UDI

Identifiers

Catalog Number
5071-140 FDA UDI
Primary DI / UDI-DI
10845854002179 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, oscillating, 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
Width — 25.4 Millimeter FDA UDI
Length — 80 Millimeter FDA UDI
Height — 1.2 Millimeter FDA UDI
Height — 0.047 Inch FDA UDI

Category: Surgical saw blade, oscillating, single-use

Me-92 by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, oscillating, 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 c7fa8f63-ee90-41d7-a25c-47be130f1ce0 36 fields · synced May 30, 2026