← Back to catalogue

Global Icon

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
GLOBAL ICON FDA UDI
Generic Name
Humeral metaphyseal anchor FDA UDI
Device Name
GLOBAL ICON Stemless Shoulder System Anchor Plate Size 48 HA FDA UDI
Model / Reference
1140-10-048 FDA UDI
Description
GLOBAL ICON Stemless Shoulder System Anchor Plate Size 48 HA FDA UDI

Identifiers

Catalog Number
114010048 FDA UDI
Primary DI / UDI-DI
10603295381129 FDA UDI
FDA Product Code
PKC FDA UDI
GMDN Term
Humeral metaphyseal anchor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Humeral metaphyseal anchor

Global Icon by Depuy (ireland) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Humeral metaphyseal anchor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI b2557a9a-e923-4385-ad4d-77dee847526e 35 fields · synced May 31, 2026