NITINOL GUIDE WIRE

GUDID M209213930

Intraoperative bone pin/screw, non-sterile

Primary Device ID	M209213930
NIH Device Record Key	8771ad78-13e9-4229-bd12-0e1c8e765e4a
Commercial Distribution Status	In Commercial Distribution
Brand Name	NITINOL GUIDE WIRE
Version Model Number	21393
Company DUNS	618749857
Company Name	BIOPRO, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
HIBCC	M209213930 [Primary]

HTY	Pin, Fixation, Smooth

Steralize Prior To Use	true
Device Is Sterile	false

[M209213930]

Moist Heat or Steam Sterilization