FDA UDI In Commercial Distribution 🇺🇸 United States

PEDIMAG BLOOD PUMP

DI: 07640135140634 · Model: 201-90052 · Thoratec Switzerland GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PEDIMAG BLOOD PUMP
Primary DI
07640135140634
Version / Model
201-90052
Catalog Number
201-90052
Company Name
Thoratec Switzerland GmbH
Labeler DUNS
486066918
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-20
Public Version
6
Public Version Date
2020-05-19
Public Version Status
Update
Public Device Record Key
c22fcb5a-230d-4430-a6f5-182951cacff7

Device Characteristics

Single Use
Yes
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
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
KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type

GMDN Terms

Code Name
31718 Cardiopulmonary bypass system centrifugal pump

Identifiers

Type ID
Primary 07640135140634

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius