UNIVERSAL F® FLEX FF376-13621Z

GUDID 00612649214962

UNIVERSAL F FLEX CIRCUIT

King Systems Corporation

Anaesthesia breathing circuit, single-use
Primary Device ID00612649214962
NIH Device Record Keyd12b9f2d-d392-4d3d-bb2e-3cf8edf46d24
Commercial Distribution StatusIn Commercial Distribution
Brand NameUNIVERSAL F® FLEX
Version Model NumberFF376-13621Z
Catalog NumberFF376-13621Z
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.com
Phone+1(410)768-6464
EmailPurchase_orders@ambuUSA.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 Identifiers

Device Issuing AgencyDevice ID
GS100612649214962 [Package]
Contains: 00612649214979
Package: [30 Units]
In Commercial Distribution
GS100612649214979 [Primary]

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 Number2
Public Version Date2026-01-30
Device Publish Date2023-01-16

On-Brand Devices [UNIVERSAL F® FLEX]

00612649213866Universal F Flex Breathing Circuit
00612649213729Universal F Flex Breathing Circuit
00612649215655UNIVERSAL F FLEX CIRCUIT PACK KIT
00612649179001UNIVERSAL F FLEX CIRCUIT
00612649180489UNIVERSAL F FLEX CIRCUIT
00612649180151UNIVERSAL F FLEX CIRCUIT
00612649214986UNIVERSAL F FLEX CIRCUIT
00612649214962UNIVERSAL F FLEX CIRCUIT
00612649210070Universal F Flex Circuit

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

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.