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Comprehensive® VRS™ Glenoid

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
Comprehensive® VRS™ Glenoid FDA UDI
Generic Name
Reverse shoulder prosthesis base plate FDA UDI
Model / Reference
110027734 FDA UDI

Identifiers

Catalog Number
110027734 FDA UDI
Primary DI / UDI-DI
00880304818934 FDA UDI
510(k) Number
K152754 FDA UDI
K202232 FDA UDI
FDA Product Code
PHX FDA UDI
GMDN Term
Reverse shoulder prosthesis base plate 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

Yes

FDA UDI

Category: Reverse shoulder prosthesis base plate

Comprehensive® VRS™ Glenoid by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reverse shoulder prosthesis base plate.

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 045b3560-63fa-4065-b006-da2c8f1a530d 36 fields · synced May 30, 2026