Sternalock (tm) System

FDA UDI

Class I (US FDA UDI)

by Biomet Microfixation, Inc

Identity

Trade Name: STERNALOCK (TM) SYSTEM FDA UDI
Generic Name: Surgical instrument/implant rack FDA UDI
Model / Reference: 71-1306 FDA UDI

Identifiers

Catalog Number: 71-1306 FDA UDI
Primary DI / UDI-DI: 00841036071011 FDA UDI
FDA Product Code: LRP FDA UDI
HWC FDA UDI
HRS FDA UDI
GMDN Term: Surgical instrument/implant rack FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
888.3040 FDA UDI
888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument/implant rack

Sternalock (tm) System by Biomet Microfixation, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Biomet Microfixation, Inc

Sources (1)

FDA UDI 92662afa-b91e-473c-a0be-425ec8c01393 34 fields · synced May 31, 2026