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Global Steptech

FDA UDI

Class I (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
GLOBAL STEPTECH FDA UDI
Generic Name
Surgical saw blade, oscillating, single-use FDA UDI
Device Name
GLOBAL STEPTECH ANCHOR PEG GLENOID STEPTECH OSCL RASP LG +7 LINV FITS: CONMED MICROFREE AND HALL MICROPOWER LARGE +7MM FDA UDI
Model / Reference
223000365 FDA UDI
Description
GLOBAL STEPTECH ANCHOR PEG GLENOID STEPTECH OSCL RASP LG +7 LINV FITS: CONMED MICROFREE AND HALL MICROPOWER LARGE +7MM FDA UDI

Identifiers

Catalog Number
223000365 FDA UDI
Primary DI / UDI-DI
10603295525424 FDA UDI
FDA Product Code
KIJ 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

No

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

Category: Surgical saw blade, oscillating, single-use

Global Steptech by Depuy (ireland) — 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
Depuy (ireland)

Sources (1)

  • FDA UDI c02d52d2-44d4-4f0d-bd3d-1529a76cbe8b 35 fields · synced Jun 8, 2026