Removal Driver

GUDID M209175500

Surgical instrument handle, non-torque-limiting

Primary Device ID	M209175500
NIH Device Record Key	4aabb44c-1410-4a0e-bedb-1fc2e0ca560a
Commercial Distribution Status	In Commercial Distribution
Brand Name	Removal Driver
Version Model Number	17149
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	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
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	M209175500 [Primary]

HXX	Screwdriver

Steralize Prior To Use	true
Device Is Sterile	false

[M209175500]

Moist Heat or Steam Sterilization