FDA UDI In Commercial Distribution 🇺🇸 United States

INTEGRAL 180 PRIMARY/REVISION PROV.

DI: 00880304308664 · Model: 31-166019 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INTEGRAL 180 PRIMARY/REVISION PROV.
Primary DI
00880304308664
Version / Model
31-166019
Catalog Number
31-166019
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-15
Public Version
1
Public Version Date
2020-05-25
Public Version Status
New
Public Device Record Key
e3e335a9-e95d-4e09-a173-27a00631fdaf

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
HWT TEMPLATE

GMDN Terms

Code Name
58481 Femoral stem prosthesis trial

Identifiers

Type ID
Primary 00880304308664

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 19.0 X 180 MM