FDA UDI In Commercial Distribution 🇺🇸 United States

CAPIOX® SP PUMP

DI: 04987350734433 · Model: XX*SP03 · TERUMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CAPIOX® SP PUMP
Primary DI
04987350734433
Version / Model
XX*SP03
Catalog Number
XX*SP03
Company Name
TERUMO CORPORATION
Labeler DUNS
690543319
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-17
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
9c725f07-6673-4d45-bf8a-1dc94eadf7e3

Device Description

SP PUMP HEAD ADAPTER

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type

GMDN Terms

Code Name
36379 Centrifugal circulatory assist pump, electric

Identifiers

Type ID
Package 54987350734438
Primary 04987350734433

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry. Keep away from sunlight.