FDA UDI In Commercial Distribution 🇺🇸 United States

MAQUET CARDIOHELP

DI: 04037691816432 · Model: BS 3/8x3/32 L1.7 · Maquet Cardiopulmonary AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAQUET CARDIOHELP
Primary DI
04037691816432
Version / Model
BS 3/8x3/32 L1.7
Catalog Number
70105.5720
Company Name
Maquet Cardiopulmonary AG
Labeler DUNS
316153865
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-10
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
7fdf76be-500b-4746-9910-f552fa70eeb1

Device Description

MAQUET CARDIOHELP Bubble Sensor BS 3/8x3/32 L1.7

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
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
35440 Cardiopulmonary bypass system air bubble/fluid level detector

Identifiers

Type ID
Primary 04037691816432

Premarket Submissions

Submission Number Supplement Number
K133598 000