FDA UDI In Commercial Distribution 🇺🇸 United States

Terumo® Advanced Perfusion System 1

DI: 00886799000656 · Model: 801763 · Terumo Cardiovascular Systems Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Terumo® Advanced Perfusion System 1
Primary DI
00886799000656
Version / Model
801763
Catalog Number
801763
Company Name
Terumo Cardiovascular Systems Corporation
Labeler DUNS
177655466
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
9db876d4-96ce-4410-8bca-948c73524609

Device Description

System base using a 100V-120V, 15A (circuit breaker), 50/60 Hz (20A power source required) power source

Device Characteristics

Single Use
No
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
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
35099 Cardiopulmonary bypass system, roller type

Identifiers

Type ID
Primary 00886799000656

Premarket Submissions

Submission Number Supplement Number
K151349 000