FDA UDI Not in Commercial Distribution 🇺🇸 United States

QUADROX-i

DI: 04058863018867 · Model: Small Adult, reservoir, filter VKMO 51000-USA #SQUADR-i HMO51000+VHK710 · Maquet Cardiopulmonary AG
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
QUADROX-i
Primary DI
04058863018867
Version / Model
Small Adult, reservoir, filter VKMO 51000-USA #SQUADR-i HMO51000+VHK710
Catalog Number
70106.7970
Company Name
Maquet Cardiopulmonary AG
Labeler DUNS
316153865
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-15
Public Version
5
Public Version Date
2024-09-30
Public Version Status
Update
Public Device Record Key
55f58c34-b4fe-4c8b-94b3-7525c752bc5b
Distribution End Date
2024-09-25

Device Description

QUADROX-i Small Adult HMO 51000 + VHK 71000 Oxygenator with venous hardshell cardiotomy reservoir, vacuum-tight

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DTP Defoamer, cardiopulmonary bypass
JOD FILTER, BLOOD, CARDIOTOMY SUCTION LINE, CARDIOPULMONARY BYPASS
DTN RESERVOIR, BLOOD, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
31710 Cardiotomy reservoir

Identifiers

Type ID
Primary 04058863018867

Customer Contacts

Phone
+49072229320