FDA UDI In Commercial Distribution 🇺🇸 United States

Oxford Partial Knee SystemFemoral Impactor

DI: 05019279477333 · Model: 32-420127 · Biomet Uk Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Oxford Partial Knee SystemFemoral Impactor
Primary DI
05019279477333
Version / Model
32-420127
Catalog Number
32-420127
Company Name
Biomet Uk Ltd
Labeler DUNS
219322575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-23
Public Version
2
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
3befd5e5-60ce-441d-9eb6-0ef233cad330

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
No
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 05019279477333

Customer Contacts