FDA UDI In Commercial Distribution 🇺🇸 United States

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DI: M209103700 · Model: 10370 · BIOPRO, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
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Primary DI
M209103700
Version / Model
10370
Company Name
BIOPRO, INC.
Labeler DUNS
618749857
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-16
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
8881e5f4-eb42-4095-a377-a3693b81ac73

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
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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 M209103700

Premarket Submissions

Submission Number Supplement Number
K904448 000