UNIVERSAL F® FLEXBREATHING CIRCUIT GHUF376-6121Z

GUDID 00612649213064

Universal F Flex Breathing Circuit

King Systems Corporation

Anaesthesia breathing circuit, single-use
Primary Device ID00612649213064
NIH Device Record Key06b89fa3-0bc5-4b6c-85a8-18b45026b173
Commercial Distribution StatusIn Commercial Distribution
Brand NameUNIVERSAL F® FLEXBREATHING CIRCUIT
Version Model NumberGHUF376-6121Z
Catalog NumberGHUF376-6121Z
Company DUNS009299017
Company NameKing Systems Corporation
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com
Phone+13177763175
Emailwnet@ambu.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100612649213057 [Primary]
GS100612649213064 [Package]
Contains: 00612649213057
Package: [50 Units]
In Commercial Distribution

FDA Product Code

CAICircuit, breathing (w connector, adaptor, y piece)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-11-27
Device Publish Date2017-12-20

On-Brand Devices [UNIVERSAL F® FLEXBREATHING CIRCUIT]

00612649213545UNIVERSAL F FLEX CIRCUIT
00612649213118Universal F Flex Breathing Circuit
00612649213071Universal F Flex Breathing Circuit
00612649213064Universal F Flex Breathing Circuit
00612649209944UNIVERSAL F FLEX CIRCUIT
00612649184296UNIVERSAL F FLEX CIRCUT 50/CS
00612649180991UNIVERSAL F FLEX CIRCUIT
00612649184227UNIVERSAL F FLEX CIRCUT 50/CS
00612649179018UNIVERSAL F FLEX CIRCUIT
00612649179568UNIVERSAL F FLEX CIRCUIT
00612649179827UNIVERSAL F FLEX CIRCUIT 50/CS

Trademark Results [UNIVERSAL F]

Mark Image

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

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.