Procedure Products Needle

GUDID B1603293572

Vascular catheter introduction needle Vascular catheter introduction needle

Primary Device ID	B1603293572
NIH Device Record Key	ac45d3f0-903d-4edd-a7bd-f589c62b70d6
Commercial Distribution Status	In Commercial Distribution
Brand Name	Procedure Products Needle
Version Model Number	329-357
Company DUNS	151507563
Company Name	PROCEDURE 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	false
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	B1603293571 [Primary]
HIBCC	B1603293572 [Package] Contains: B1603293571 Package: Box [25 Units] In Commercial Distribution

DRE	Dilator, Vessel, For Percutaneous Catheterization

Steralize Prior To Use	false
Device Is Sterile	true