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Comprehensive Shoulder System

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
COMPREHENSIVE SHOULDER SYSTEM FDA UDI
Generic Name
Coated shoulder humeral stem prosthesis FDA UDI
Model / Reference
113626 FDA UDI

Identifiers

Catalog Number
113626 FDA UDI
Primary DI / UDI-DI
00880304449770 FDA UDI
510(k) Number
K060692 FDA UDI
FDA Product Code
HSD FDA UDI
KWT FDA UDI
MBF FDA UDI
KWS FDA UDI
GMDN Term
Coated shoulder humeral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3650 FDA UDI
888.3670 FDA UDI
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

Category: Coated shoulder humeral stem prosthesis

Comprehensive Shoulder System by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated shoulder humeral stem prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e2a6ef06-302a-46f6-a064-f70fbf297ed8 36 fields · synced May 30, 2026