FDA UDI In Commercial Distribution 🇺🇸 United States

Guide Wire Subtalar 8

DI: M209172300 · Model: 17230 · BIOPRO, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Guide Wire Subtalar 8
Primary DI
M209172300
Version / Model
17230
Company Name
BIOPRO, INC.
Labeler DUNS
618749857
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-27
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
39c2adb3-83cc-49b3-a22d-3cd78bcfe97b

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Primary M209172300