FDA UDI Not in Commercial Distribution 🇺🇸 United States

QUADROX-i

DI: 04037692009987 · Model: Adult, reservoir · Maquet Cardiopulmonary AG
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
QUADROX-i
Primary DI
04037692009987
Version / Model
Adult, reservoir
Catalog Number
70106.7945
Company Name
Maquet Cardiopulmonary AG
Labeler DUNS
316153865
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-15
Public Version
4
Public Version Date
2020-01-22
Public Version Status
Update
Public Device Record Key
0d57e9a8-d882-42ff-b3f9-e94e234ae05d
Distribution End Date
2017-02-16

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 04037692009987

Customer Contacts

Phone
+49072229320

Premarket Submissions

Submission Number Supplement Number
K132166 000