AccessGUDID - DEVICE: QUADROX-i (04058863019079)

GUDID

Device Identifier (DI) Information

Brand Name: QUADROX-i
Version or Model: BEQ-HMO 50000-USA #SQUADR-i Small Ado.Fi / Small Adult, BIOLINE
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 70106.7905
Company Name: Maquet Cardiopulmonary AG

Primary DI Number: 04058863019079
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 316153865 *Terms of Use

Device Description: QUADROX-i Small Adult Microporous Membrane Oxygenator, BIOLINE coated, without filter, with a screw connector

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
17643	Extracorporeal membrane oxygenator	A device designed for the extracorporeal diffusion of oxygen into blood across a gas-permeable membrane during a cardiopulmonary bypass or extracorporeal membrane oxygenation procedure. It includes a membrane that separates a thin layer of blood from the oxygenating gas; oxygen diffuses from the gas compartment into the blood, while carbon dioxide diffuses from the blood through the membrane and is flushed out of the oxygenator by the oxygen flow. The device may include an integrated heat exchanger, arterial filter, or cardiotomy/venous reservoir. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DTZ	OXYGENATOR, CARDIOPULMONARY BYPASS
DTR	HEAT-EXCHANGER, CARDIOPULMONARY BYPASS
DTM	Filter, blood, cardiopulmonary bypass, arterial line

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K150267	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: af55c75d-1073-4309-a28d-5ed973b99b1a
Public Version Date: January 22, 2020
Public Version Number: 4
DI Record Publish Date: February 16, 2017