Mask, Value, Medium Adult 1955

GUDID 00612649185255

MASK,VALUE,MEDIUM ADULT

King Systems Corporation

Anaesthesia face mask, single-use
Primary Device ID00612649185255
NIH Device Record Keye1d05ed4-8b2c-43fa-90b4-a4c61ba2114f
Commercial Distribution StatusIn Commercial Distribution
Brand NameMask, Value, Medium Adult
Version Model Number1955
Catalog Number1955
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 Datefalse
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
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Device Identifiers

Device Issuing AgencyDevice ID
GS100612649168166 [Package]
Package: [50 Units]
In Commercial Distribution
GS100612649185255 [Primary]

FDA Product Code

BSJMASK, GAS, ANESTHETIC

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 Date2022-12-08

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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

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