ADULT ULTRA FLEX®ANESTHESIA BREATHING CIRCUIT

Primary DI
00612649159935
Brand
ADULT ULTRA FLEX®ANESTHESIA BREATHING CIRCUIT
Company
King Systems Corporation
Model
5903F-13221Z
Catalog number
5903F-13221Z
Device description
Adult Ultraflex Circuit 30/CS
Published
2016-09-22
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
CAICircuit, breathing (w connector, adaptor, y piece)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
CAICircuit, Breathing (W Connector, Adaptor, Y Piece)Anesthesiology1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00612649159935PackageGS130In Commercial Distribution
00612649190488PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00612649159935006126491599356126491599350612649159935
00612649190488006126491904886126491904880612649190488

GMDN Terms#

Term, Definition table
TermDefinition
Anaesthesia breathing circuit, single-useAn assembly of devices designed to conduct medical gases from the fresh gas supply outlet of an anaesthesia unit/workstation to the patient, typically connecting the patient, a ventilator/ventilation bag, carbon dioxide (CO2) absorber, and a monitor. It typically includes both an inhalation and exhalation route and consists of breathing tubes, a ventilation and/or reservoir bag(s), a Y-piece, connectors/adaptors, and gas sampling ports. The absorber, a one-way directional valve, and adjustable pressure limiting (APL) valve are also devices typically employed in the circuit but may not be a part of this device. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+14107686464Purchase_orders@ambuUSA.com
+1(410)768-6464Purchase_orders@ambuUSA.com

Regulatory Flags#

DUNS number
009299017
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00612649214559UNIVERSAL F® FLEX2®AF476-6121ZAF476-6121Z2023-01-18
00612649100494CORRUGATED TUBING1011001011002022-12-18
00612649185224WASHINGTON CONNECTOR178517852022-12-08
00612649106779100 FT 22MM ULTRA FLEX® TUBING30010300102022-12-18
00612649121758100 FT., 6" 22MM SEGMENTEDB101100B1011002022-12-08
00612649149103RE'SPOSABLE® F2®MD121MD1212022-12-08
0061264915411418" REUSABLE TUBINGMD124MD1242022-12-08
00612649190242BREATHING BAG514551452022-12-08
00612649190181BREATHING BAG513751372022-12-08
00612649190211BREATHING BAG514151412022-12-08
00612649190198BREATHING BAG513951392022-12-08
00612649190136BREATHING BAG510951092022-12-08
00612649190112BREATHING BAG510751072022-12-08
00612649190105BREATHING BAG510551052022-12-08
00612649190129BREATHING BAG510851082022-12-08
00612649190099BREATHING BAG510151012022-12-08
00612649190068BREATHING BAG509750972022-12-08
00612649190075BREATHING BAG509850982022-12-08
00612649190082BREATHING BAG509950992022-12-08
00612649190044BREATHING BAG509450942022-12-08

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