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Anatomical Shoulder™ Combined

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Anatomical Shoulder™ Combined FDA UDI
Generic Name
Total shoulder prosthesis FDA UDI
Device Name
AS™ B/F® adaptor 45° FDA UDI
Model / Reference
01.04250.045 FDA UDI
Description
AS™ B/F® adaptor 45° FDA UDI

Identifiers

Primary DI / UDI-DI
00889024287877 FDA UDI
510(k) Number
K103404 FDA UDI
FDA Product Code
HSD FDA UDI
KWS FDA UDI
KWT FDA UDI
GMDN Term
Total shoulder prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3660 FDA UDI
888.3650 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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Angle — 45 degree FDA UDI

Category: Total shoulder prosthesis

Anatomical Shoulder™ Combined 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 c59e4c5a-0822-441c-8721-74b73859657f 36 fields · synced May 30, 2026