FDA UDI In Commercial Distribution 🇺🇸 United States

CAPIOX®FX

DI: 04987350701022 · Model: CX*FX25RE · TERUMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CAPIOX®FX
Primary DI
04987350701022
Version / Model
CX*FX25RE
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
fdddf48e-168f-4b59-a5f2-2a319e9bb77c

Device Description

FX25

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
DTZ Oxygenator, Cardiopulmonary Bypass

GMDN Terms

Code Name
17643 Extracorporeal membrane oxygenator

Identifiers

Type ID
Primary 04987350701022

Customer Contacts

Device Sizes

Type Value Unit Text
Area/Surface Area 2.5 Square meter

Storage Conditions

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