Procedure products lines

GUDID B160P12R1872

Intravenous line recessed-needle connector

Primary Device ID	B160P12R1872
NIH Device Record Key	1cac1155-a0a4-47b1-9500-9991bdde409c
Commercial Distribution Status	In Commercial Distribution
Brand Name	Procedure products lines
Version Model Number	P12-R187
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	B160P12R1871 [Primary]
HIBCC	B160P12R1872 [Package] Contains: B160P12R1871 Package: Box [25 Units] In Commercial Distribution

DQO	Catheter, Intravascular, Diagnostic

Steralize Prior To Use	false
Device Is Sterile	true

B160P24R1871	High pressure swivel line, 24"
B160P12R1872	High pressure swivel line
B160MM721	Pressure Line, 72", Male-Male
B160MM481	Pressure Line, 48", male & male
B160MM361	Pressure Line, 36", Male-Male
B160MF241	LINE, MALE/FEMALE-24 IN.
B160MF121	Pressure line, 12", male & female
B160MF061	Pressure Line, 6", male & female
B160B72R0722	High pressure braided swivel line set
B160B72F712	HIGH PRESSURE, 72" BRAIDED LINE
B160B48F0711	Fixed, braided, high-pressure connector
B160B36F711	Fixed, braided, high-pressure connector
B160B10R0721	HIGH PRESSURE BRAIDED SWIVEL LINE, 10"