FDA UDI In Commercial Distribution 🇺🇸 United States

MAQUET CARDIOHELP

DI: 04058863074863 · Model: CARDIOHELP-i · Maquet Cardiopulmonary AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAQUET CARDIOHELP
Primary DI
04058863074863
Version / Model
CARDIOHELP-i
Catalog Number
70107.2780
Company Name
Maquet Cardiopulmonary AG
Labeler DUNS
316153865
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-01
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
aad2ac39-8aa0-4bc5-abfc-c48725cdc659

Device Description

The CARDIOHELP System is a blood oxygenation and carbon dioxide removal system used to pump blood through the extracorporeal bypass circuit for circulatory and/or pulmonary support for periods appropriate to cardiopulmonary bypass (up to six hours). It is also intended to provide circulatory and/or pulmonary support during procedures not requiring cardiopulmonary bypass (for periods up to six hours). The CARDIOHELP System in configuration with the HLS/HIT Set Advanced is intended to be used within the hospital environment and outside the hospital environment (for periods up to six hours), e.g. for intra- and inter-Hospital transport. The CARDIOHELP System in configuration with the QUADROX-iR is intended to be used in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery (for periods for up to six hours).

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DTQ CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
35099 Cardiopulmonary bypass system, roller type

Identifiers

Type ID
Primary 04058863074863

Customer Contacts

Phone
+49072229320

Premarket Submissions

Submission Number Supplement Number
K133598 000