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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
Orthopaedic implant aiming/guiding block, reusable FDA UDI
Model / Reference
31-406997 FDA UDI

Identifiers

Catalog Number
31-406997 FDA UDI
Primary DI / UDI-DI
00880304539778 FDA UDI
510(k) Number
K182516 FDA UDI
FDA Product Code
PKC FDA UDI
GMDN Term
Orthopaedic implant aiming/guiding block, reusable 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implant aiming/guiding block, reusable

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

Similar devices

Also classified as Orthopaedic implant aiming/guiding block, reusable.

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 05099185-c2d0-41d5-88ea-a0177bee29b3 36 fields · synced May 29, 2026