FDA UDI In Commercial Distribution 🇺🇸 United States

BioPro

DI: M20922798 · Model: 22798 · BIOPRO, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
BioPro
Primary DI
M20922798
Version / Model
22798
Company Name
BIOPRO, INC.
Labeler DUNS
618749857
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-10
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
3cb16f73-704c-40a2-98bd-c270af191a84

Device Description

Horizon Subtalar 8" Packaged Non Sterile

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
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
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Primary M20922798