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Global Cap

FDA UDI

Class I (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
GLOBAL CAP FDA UDI
Generic Name
Orthopaedic bur, reusable FDA UDI
Device Name
GLOBAL CAP HUMERAL HEAD SHAPER 48mm x 18mm FDA UDI
Model / Reference
2230-81-050 FDA UDI
Description
GLOBAL CAP HUMERAL HEAD SHAPER 48mm x 18mm FDA UDI

Identifiers

Catalog Number
223081050 FDA UDI
Primary DI / UDI-DI
10603295105046 FDA UDI
FDA Product Code
HTO FDA UDI
GMDN Term
Orthopaedic bur, reusable 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 bur, reusable

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

Similar devices

Also classified as Orthopaedic bur, reusable.

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 eb860035-5f51-4581-9045-8a4cd7410bb0 35 fields · synced Jun 8, 2026