FDA UDI In Commercial Distribution 🇺🇸 United States

BIO-PUMP®

DI: 00613994406934 · Model: 95171 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BIO-PUMP®
Primary DI
00613994406934
Version / Model
95171
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-25
Public Version
4
Public Version Date
2020-05-19
Public Version Status
Update
Public Device Record Key
d7be8d9d-84ce-4192-bd8e-e91ad1fa5ea5

Device Description

PUMP 95171 BIOPUMP BP50 STER 3L 4PK

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KFM PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE

GMDN Terms

Code Name
31718 Cardiopulmonary bypass system centrifugal pump

Identifiers

Type ID
Package 20613994406938
Primary 00613994406934

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K852807 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 50 Degrees Celsius