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High Mobility Mini Humeral Bearing Trial 36mm STD

FDA UDI

Class I (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
High Mobility Mini Humeral Bearing Trial 36mm STD FDA UDI
Generic Name
Reverse shoulder cup prosthesis trial, reusable FDA UDI
Model / Reference
SSI007237 FDA UDI

Identifiers

Catalog Number
SSI007237 FDA UDI
Primary DI / UDI-DI
00889024657267 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Reverse shoulder cup prosthesis trial, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Reverse shoulder cup prosthesis trial, reusable

High Mobility Mini Humeral Bearing Trial 36mm STD by Zimmer, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reverse shoulder cup prosthesis trial, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI d143d9e0-b519-40da-8f4d-7a0863a5a4b9 35 fields · synced May 31, 2026