FDA UDI In Commercial Distribution 🇺🇸 United States

CAPIOX® VENOUS RESERVOIR

DI: 04987350706690 · Model: CX*VRA1001T2 · TERUMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CAPIOX® VENOUS RESERVOIR
Primary DI
04987350706690
Version / Model
CX*VRA1001T2
Company Name
TERUMO CORPORATION
Labeler DUNS
690543319
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-15
Public Version
3
Public Version Date
2020-01-22
Public Version Status
Update
Public Device Record Key
a1c06c77-3a3d-4a54-985f-fef939f43b4f

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line

GMDN Terms

Code Name
31710 Cardiotomy reservoir

Identifiers

Type ID
Package 34987350706691
Primary 04987350706690

Customer Contacts

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
1 – 40 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Fragile. This way up. Keep away from sunlight. Keep away from rain.