FDA UDI In Commercial Distribution 🇺🇸 United States

COMPREHENSIVE

DI: 00880304532298 · Model: 405809 · Biomet Orthopedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COMPREHENSIVE
Primary DI
00880304532298
Version / Model
405809
Catalog Number
405809
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-27
Public Version
6
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
cf6672d9-1123-4a89-81e2-79eaab77f60c

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
No
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
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
PHX shoulder prosthesis, reverse configuration

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 00880304532298

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120121 000
K132239 000
K193373 000

Device Sizes

Type Value Unit Text
Device Size Text, specify MINI GLENOID BASEPLATE IMPACTOR