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Global Advantage

FDA UDI

Class I (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
GLOBAL ADVANTAGE FDA UDI
Generic Name
Humeral head prosthesis trial, reusable FDA UDI
Device Name
GLOBAL ADVANTAGE HUMERAL HEAD TRIAL 52mm x 21mm FDA UDI
Model / Reference
2128-52-020 FDA UDI
Description
GLOBAL ADVANTAGE HUMERAL HEAD TRIAL 52mm x 21mm FDA UDI

Identifiers

Catalog Number
212852020 FDA UDI
Primary DI / UDI-DI
10603295088943 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Humeral head prosthesis trial, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 FDA UDI
Commercial Distribution
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b99ce481-5803-4b01-b879-7bcb2ca4ed8e 36 fields · synced Jun 8, 2026