FDA UDI In Commercial Distribution 🇺🇸 United States

COMPRESS PROXIMAL FEMORAL TRIAL

DI: 00880304610682 · Model: 32-481105 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COMPRESS PROXIMAL FEMORAL TRIAL
Primary DI
00880304610682
Version / Model
32-481105
Catalog Number
32-481105
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-09
Public Version
2
Public Version Date
2022-03-22
Public Version Status
Update
Public Device Record Key
2d88a427-884b-44ea-a5bc-5b0d84f5519c

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
HWT TEMPLATE

GMDN Terms

Code Name
58715 Knee femur prosthesis trial, reusable

Identifiers

Type ID
Primary 00880304610682

Customer Contacts