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Anatomical Shoulder™

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Anatomical Shoulder™ FDA UDI
Generic Name
Total shoulder prosthesis FDA UDI
Device Name
Humeral Stem cemented Ø10.5-100 FDA UDI
Model / Reference
01.04211.103 FDA UDI
Description
Humeral Stem cemented Ø10.5-100 FDA UDI

Identifiers

Primary DI / UDI-DI
00889024274785 FDA UDI
510(k) Number
K142403 FDA UDI
FDA Product Code
PHX FDA UDI
KWT FDA UDI
HSD FDA UDI
KWS FDA UDI
GMDN Term
Total shoulder prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3650 FDA UDI
888.3690 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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 100 Millimeter FDA UDI
Outer Diameter — 10.5 Millimeter FDA UDI

Category: Total shoulder prosthesis

Anatomical Shoulder™ by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total shoulder prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI bf77d7fe-c815-4a1d-9cd9-0db5d14c6a2d 36 fields · synced Jun 8, 2026