UNIVERSAL F® FLEX KNFF3116-6121Z

GUDID 00612649213729

Anaesthesia breathing circuit, single-use

Primary Device ID	00612649213729
NIH Device Record Key	9dddee70-f194-433f-9363-08307d714438
Commercial Distribution Status	In Commercial Distribution
Brand Name	UNIVERSAL F® FLEX
Version Model Number	KNFF3116-6121Z
Catalog Number	KNFF3116-6121Z
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	true
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	00612649213729 [Package] Contains: 00612649213736 Package: [40 Units] In Commercial Distribution
GS1	00612649213736 [Primary]

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

Steralize Prior To Use	false
Device Is Sterile	false

00612649213866	Universal F Flex Breathing Circuit
00612649213729	Universal F Flex Breathing Circuit
00612649215655	UNIVERSAL F FLEX CIRCUIT PACK KIT
00612649179001	UNIVERSAL F FLEX CIRCUIT
00612649180489	UNIVERSAL F FLEX CIRCUIT
00612649180151	UNIVERSAL F FLEX CIRCUIT

Mark Image Registration \| Serial	Company Trademark Application Date
UNIVERSAL F 74475379 1884793 Live/Registered	KING SYSTEMS CORPORATION 1994-01-03
UNIVERSAL F 74323503 not registered Dead/Abandoned	King Systems- Division of Burco Molding, Inc. 1992-10-19