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mymobility® Platform

FDA UDI

Class I (US FDA UDI)

by Zimmer Us, Inc.

Identity

Trade Name
mymobility® Platform FDA UDI
Generic Name
Biomechanical function analysis/rehabilitation software FDA UDI
Model / Reference
MMCWE001 FDA UDI

Identifiers

Catalog Number
MMCWE001 FDA UDI
Primary DI / UDI-DI
00887868581151 FDA UDI
FDA Product Code
KQW FDA UDI
GMDN Term
Biomechanical function analysis/rehabilitation software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1520 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Biomechanical function analysis/rehabilitation software

mymobility® Platform by Zimmer Us, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biomechanical function analysis/rehabilitation software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer Us, Inc.

Sources (1)

  • FDA UDI b8a1dd70-c3fa-456e-8ad5-5a658da5cbda 34 fields · synced May 30, 2026