FDA UDI In Commercial Distribution 🇺🇸 United States

U-Motion II

DI: 04719872179276 · Model: 9206-1103 · UNITED ORTHOPEDIC CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
U-Motion II
Primary DI
04719872179276
Version / Model
9206-1103
Catalog Number
9206-1103
Company Name
UNITED ORTHOPEDIC CORP.
Labeler DUNS
656700556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-02
Public Version
2
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
68e622cd-4a87-4783-9159-5fdd0db6441e

Device Description

Cup impactor

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
HWA Impactor

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 04719872179276

Customer Contacts