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Global Ap

FDA UDI

Class I (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
GLOBAL AP FDA UDI
Generic Name
Orthopaedic implant/instrument dismantling device FDA UDI
Device Name
GLOBAL AP BROACH REMOVAL TOOL FDA UDI
Model / Reference
2130-01-085 FDA UDI
Description
GLOBAL AP BROACH REMOVAL TOOL FDA UDI

Identifiers

Catalog Number
213001085 FDA UDI
Primary DI / UDI-DI
10603295090601 FDA UDI
FDA Product Code
HTQ FDA UDI
GMDN Term
Orthopaedic implant/instrument dismantling device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implant/instrument dismantling device

Global Ap by Depuy Orthopaedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant/instrument dismantling device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy Orthopaedics, Inc.

Sources (1)

  • FDA UDI afa42b50-fbca-4ef0-a460-6d6d7c87cdde 35 fields · synced Jun 8, 2026