Director Sterile Disposable Needle Guide 4023

GUDID 10841912101075

Nonimplantable needle guide, single-use

Primary Device ID	10841912101075
NIH Device Record Key	dfb2c028-c812-48eb-b591-735736b51a6c
Commercial Distribution Status	In Commercial Distribution
Brand Name	Director Sterile Disposable Needle Guide
Version Model Number	4023
Catalog Number	4023
Company DUNS	965417181
Company Name	PROTEK MEDICAL PRODUCTS, 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	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00841912101078 [Primary]
GS1	10841912101075 [Package] Contains: 00841912101078 Package: [24 Units] In Commercial Distribution

ITX	Transducer, Ultrasonic, Diagnostic

Steralize Prior To Use	false
Device Is Sterile	true