Reunion

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: REUNION FDA UDI
Generic Name: Glenoid orthopaedic reamer FDA UDI
Device Name: Cannulated Glenoid Reamer Size 44 FDA UDI
Model / Reference: 5901-6075 FDA UDI
Description: Cannulated Glenoid Reamer Size 44 FDA UDI

Identifiers

Catalog Number: 5901-6075 FDA UDI
Primary DI / UDI-DI: 07613327292428 FDA UDI
FDA Product Code: HSD FDA UDI
KWS FDA UDI
PHX FDA UDI
GMDN Term: Glenoid orthopaedic reamer FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3690 FDA UDI
888.3660 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: Glenoid orthopaedic reamer

Reunion by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Glenoid orthopaedic reamer.

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Alliance — Zimmer, Inc. · Class II
PRIMA TT Glenoid — Limacorporate · Class II
OFF AXIS COMP MINI REAMER 6-SPOKE LG — Biomet Orthopedics, Inc. · Class II
Equinoxe — Exactech, Inc. · Class II
Equinoxe — Exactech, Inc. · Class II

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 II	Pending data

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Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI c892ec03-12d2-4334-b1bb-9bc223f196ff 34 fields · synced May 30, 2026