2 LITER CONTOUR® 30902Z

GUDID 00612649140834

BAG,2 LITER CONTOUR LATEX FREE

King Systems Corporation

Breathing circuit bag, single-use
Primary Device ID00612649140834
NIH Device Record Keyba9d850d-1b97-4305-b3c9-855b5e52f0bd
Commercial Distribution StatusIn Commercial Distribution
Brand Name2 LITER CONTOUR®
Version Model Number30902Z
Catalog Number30902Z
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 Kitfalse
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+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
GS100612649140834 [Package]
Contains: 00612649188225
Package: [30 Units]
In Commercial Distribution
GS100612649188225 [Primary]

FDA Product Code

BTCBAG, RESERVOIR

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 Date2022-12-13

Devices Manufactured by King Systems Corporation

00612649214559 - UNIVERSAL F® FLEX2®2026-02-02 UNIVERSAL F FLEX2 CIRCUIT
00612649100494 - CORRUGATED TUBING2026-01-30 TUBING,100' SEGMENTED COIL
00612649185224 - WASHINGTON CONNECTOR2026-01-30 CUSTOM ACCESSORY
00612649106779 - 100 FT 22MM ULTRA FLEX® TUBING2026-01-30 TUBING 100 ULTRAFLEX COIL
00612649121758 - 100 FT., 6" 22MM SEGMENTED2026-01-30 TUBING 100 SEGMENTED COIL
00612649149103 - RE'SPOSABLE® F2®2026-01-30 RESPOSABLE F2 PLASTIC MANIFOLD
00612649154114 - 18" REUSABLE TUBING2026-01-30 TUBING,18"REUSEABLE CREAM
00612649190242 - BREATHING BAG2026-01-30 BREATHING BAG,3L,NEOPRENE

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