FDA UDI In Commercial Distribution 🇺🇸 United States

BKS TriMax PS Plus

DI: 00822409124503 · Model: 166-8108 · Ortho Development Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BKS TriMax PS Plus
Primary DI
00822409124503
Version / Model
166-8108
Company Name
Ortho Development Corporation
Labeler DUNS
876542390
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-01
Public Version
1
Public Version Date
2023-11-09
Public Version Status
New
Public Device Record Key
779c4f94-7da1-44c5-a135-1bd8eca676d9

Device Description

PS Plus Insert Size 1 8mm SFP

Device Characteristics

Single Use
Yes
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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
46585 Tibial insert

Identifiers

Type ID
Primary 00822409124503

Customer Contacts

Device Sizes

Type Value Unit Text
Height 8 Millimeter