← Back to catalogue

GLOBAL ICON Stemless Shoulder System

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2240-13-052Model Bone-coring Punch, Reusable

by DePuy Ireland UC

Identity

Trade Name
GLOBAL ICON Stemless Shoulder System EUDAMED
GLOBAL ICON FDA UDI
Generic Name
Bone-coring punch, reusable FDA UDI
Device Name
Bone-coring Punch, Reusable EUDAMED
GLOBAL ICON Stemless Shoulder System HUMERAL PUNCH Size 52 FDA UDI
Model / Reference
Bone-coring Punch, Reusable EUDAMED
2240-13-052 EUDAMEDFDA UDI
Description
GLOBAL ICON Stemless Shoulder System HUMERAL PUNCH Size 52 FDA UDI

Identifiers

Catalog Number
224013052 FDA UDI
Primary DI / UDI-DI
10603295425380 EUDAMEDFDA UDI
Basic UDI-DI
0603295a004148M EUDAMED
Direct Marketing DI
10603295425380 EUDAMED
FDA Product Code
HTZ FDA UDI
EMDN Code
L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Bone-coring punch, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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: Bone cutting forceps, reusable

GLOBAL ICON Stemless Shoulder System by DePuy Ireland UC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutting forceps, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
DePuy Ireland UC
EUDAMED SRN
IE-MF-000007377

Sources (2)

  • EUDAMED 83d8ec31-a125-44af-86ba-86de79cae55d 61 fields · synced Jul 17, 2026
  • FDA UDI e99d142e-73ab-493c-bdb9-7a417f341c80 35 fields · synced May 30, 2026