FDA UDI In Commercial Distribution 🇺🇸 United States

HLS Set

DI: 04058863080383 · Model: BEQ-HLS 7050 USA · Maquet Cardiopulmonary AG
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HLS Set
Primary DI
04058863080383
Version / Model
BEQ-HLS 7050 USA
Catalog Number
701069078
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
2
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
5e001841-a422-4a15-8f1f-bb6b0735a37d

Device Description

HLS Set Advanced 7.0, Adult, 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
DTZ Oxygenator, Cardiopulmonary Bypass
DTR Heat-Exchanger, Cardiopulmonary Bypass
KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Primary 04058863080383

Premarket Submissions

Submission Number Supplement Number
K112360 000

Device Sizes

Type Value Unit Text
Total Volume 600 Milliliter
Device Size Text, specify Connection size 3/8 Inch