FDA UDI In Commercial Distribution 🇺🇸 United States

mymobility® Platform

DI: 00887868574283 · Model: MMAND001 · Zimmer Us, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
mymobility® Platform
Primary DI
00887868574283
Version / Model
MMAND001
Catalog Number
MMAND001
Company Name
Zimmer Us, Inc.
Labeler DUNS
117672130
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-16
Public Version
2
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
93338863-54c2-4ac0-a384-af0e6dc10558

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KQW Goniometer, nonpowered

GMDN Terms

Code Name
47518 Biomechanical function analysis/rehabilitation software

Identifiers

Type ID
Primary 00887868574283

Customer Contacts