FDA UDI In Commercial Distribution 🇺🇸 United States

Abiomed Breethe OXY-1 System

DI: 00860001797954 · Model: 001-0901-003 · Breethe, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Abiomed Breethe OXY-1 System
Primary DI
00860001797954
Version / Model
001-0901-003
Catalog Number
001-0901-007
Company Name
Breethe, Inc.
Labeler DUNS
079455574
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-30
Public Version
3
Public Version Date
2023-06-20
Public Version Status
Update
Public Device Record Key
7872eb1b-c96e-405b-9651-dec388bbc4ff

Device Description

E-Drive Assembly

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
DTZ Oxygenator, Cardiopulmonary Bypass

GMDN Terms

Code Name
46838 Cardiopulmonary bypass system, non-roller type

Identifiers

Type ID
Primary 00860001797954

Premarket Submissions

Submission Number Supplement Number
K223161 000