FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 04037692009932 · Model: QUADROX-iD Adult, BIOLINE Coating · Maquet Cardiopulmonary AG
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04037692009932
Version / Model
QUADROX-iD Adult, BIOLINE Coating
Catalog Number
70106.7859
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
20b6622b-d6b4-48f4-8c9c-44107a4cb837
Distribution End Date
2017-02-16

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
DTM Filter, blood, cardiopulmonary bypass, arterial line
DTZ OXYGENATOR, CARDIOPULMONARY BYPASS
DTR HEAT-EXCHANGER, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
17643 Extracorporeal membrane oxygenator

Identifiers

Type ID
Primary 04037692009932

Customer Contacts

Phone
+49072229320

Premarket Submissions

Submission Number Supplement Number
K150267 000

Device Sizes

Type Value Unit Text
Total Volume 215 Milliliter