UNIVERSAL F2® C0120-230

GUDID 00612649142593

Anaesthesia breathing circuit, single-use

Primary Device ID	00612649142593
NIH Device Record Key	fed76423-9e46-4609-ae33-1722f27a2a8e
Commercial Distribution Status	In Commercial Distribution
Brand Name	UNIVERSAL F2®
Version Model Number	C0120-230
Catalog Number	C0120-230
Company DUNS	009299017
Company Name	King Systems Corporation
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00612649142593 [Package] Contains: 00612649200033 Package: [15 Units] In Commercial Distribution
GS1	00612649200033 [Primary]

CAI	Circuit, breathing (w connector, adaptor, y piece)

Steralize Prior To Use	false
Device Is Sterile	false

Mark Image Registration \| Serial	Company Trademark Application Date
UNIVERSAL F2 75354132 2336533 Live/Registered	King Systems Corporation 1997-09-09