FDA UDI In Commercial Distribution 🇺🇸 United States

Quadrox-iD

DI: 04058863154435 · Model: BEQ-HMOD30000-USA · Maquet Cardiopulmonary AG
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Quadrox-iD
Primary DI
04058863154435
Version / Model
BEQ-HMOD30000-USA
Catalog Number
701070397
Company Name
Maquet Cardiopulmonary AG
Labeler DUNS
316153865
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-29
Public Version
1
Public Version Date
2021-08-06
Public Version Status
New
Public Device Record Key
aa4ea870-1082-4592-8fb2-08b274bc7bbf

Device Description

QUADROX-iD Pediatric with BIOLINE Coating

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
DTR Heat-Exchanger, Cardiopulmonary Bypass
DTZ Oxygenator, Cardiopulmonary Bypass

GMDN Terms

Code Name
17643 Extracorporeal membrane oxygenator

Identifiers

Type ID
Package 04058863299983
Primary 04058863154435

Premarket Submissions

Submission Number Supplement Number
K132829 000