FDA UDI In Commercial Distribution 🇺🇸 United States

EXACT/ALLIANCE BROACH PROVISIONAL

DI: 00880304183247 · Model: X31-400009 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EXACT/ALLIANCE BROACH PROVISIONAL
Primary DI
00880304183247
Version / Model
X31-400009
Catalog Number
X31-400009
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-28
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
88c6d715-fa16-43f5-9d93-4f8f9b0a01cd

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
58481 Femoral stem prosthesis trial

Identifiers

Type ID
Primary 00880304183247

Customer Contacts