UNIVERSAL F® FLEX2® KNAF270-6121Z

GUDID 00612649216423

UNIVERSAL F FLEX2 CIRCUIT

King Systems Corporation

Anaesthesia breathing circuit, single-use
Primary Device ID00612649216423
NIH Device Record Key8c893e63-1643-43bd-8b65-9e84b5af3e0e
Commercial Distribution StatusIn Commercial Distribution
Brand NameUNIVERSAL F® FLEX2®
Version Model NumberKNAF270-6121Z
Catalog NumberKNAF270-6121Z
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com
Phone+14107686464
EmailPurchase_orders@ambuUSA.com

Device Dimensions

Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter
Lumen/Inner Diameter2 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter5 Millimeter
Length350 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100612649216423 [Package]
Contains: 00612649216430
Package: [40 Units]
In Commercial Distribution
GS100612649216430 [Primary]

FDA Product Code

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

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-05-26
Device Publish Date2023-05-18

On-Brand Devices [UNIVERSAL F® FLEX2®]

00612649215167UNIVERSAL F FLEX2 CIRCUIT
00612649215488UNIVERSAL F FLEX2 CIRCUIT
00612649215464UNIVERSAL F FLEX2 CIRCUIT
00612649215914UNIVERSAL FLEX2 CIRCUIT
00612649215877UNIVERSAL F FLEX2 CIRCUIT
00612649216447Universal F Flex Breathing Circuit
00612649216423UNIVERSAL F FLEX2 CIRCUIT
00612649216409UNIVERSAL F FLEX2 CIRCUIT
00612649216386UNIVERSAL F FLEX2 CIRCUIT & Pack Kit

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

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