FDA UDI In Commercial Distribution 🇺🇸 United States

U2™ Knee

DI: 04719872175018 · Model: 9303-5104-RA · UNITED ORTHOPEDIC CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
U2™ Knee
Primary DI
04719872175018
Version / Model
9303-5104-RA
Catalog Number
9303-5104-RA
Company Name
UNITED ORTHOPEDIC CORP.
Labeler DUNS
656700556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-29
Public Version
3
Public Version Date
2018-05-31
Public Version Status
Update
Public Device Record Key
509aab55-51a7-4b56-b224-4ee7752fab66

Device Description

PS Housing punch

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
HWP Punch, Femoral Neck

GMDN Terms

Code Name
12844 Orthopaedic osteotome

Identifiers

Type ID
Primary 04719872175018

Customer Contacts