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Reunion

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
REUNION FDA UDI
Generic Name
Reverse shoulder prosthesis head FDA UDI
Device Name
GLENOSPHERE , 2mm ECCENTRIC FDA UDI
Model / Reference
5573-2E-3602 FDA UDI
Description
GLENOSPHERE , 2mm ECCENTRIC FDA UDI

Identifiers

Catalog Number
5573-2E-3602 FDA UDI
Primary DI / UDI-DI
07613327098914 FDA UDI
FDA Product Code
KWS FDA UDI
GMDN Term
Reverse shoulder prosthesis head 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

No

FDA UDI

Category: Reverse shoulder prosthesis head

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

Similar devices

Also classified as Reverse shoulder prosthesis head.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI e4483030-ef0e-45d1-92a1-d29c64d410a2 35 fields · synced Jun 8, 2026