DEVICE: CAPIOX (04987350705730)

Download: XML | JSON

Device Identifier (DI) Information

CAPIOX
CX*BT15

TERUMO CORPORATION
04987350705730
GS1
1
CAPIOX Bubble Trap
CLOSE

Device Characteristics

Labeling does not contain MRI Safety Information
No
No
Yes
Yes
No
No
No
No

GMDN

[?]

GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name GMDN Definition
Cardiopulmonary bypass system defoamer A sterile device that is used remove gas bubbles from the blood during cardiopulmonary bypass surgery and is used in conjunction with an oxygenator [the device used to add the necessary oxygen (O2) to the blood before being returned back to the patient]. This is a single-use device.
CLOSE

FDA Product Code

[?]
Product Code Product Code Name
KRL DETECTOR, BUBBLE, CARDIOPULMONARY BYPASS
CLOSE

Sterilization

Yes
No
Sterilization Method [?]
No Sterilization Methods Found
CLOSE

Storage and Handling

[?]
Storage and Handling
Handling Environment Temperature: between 1 and 40 Degrees Celsius
Special Storage Condition, Specify: Keep away from rain.
Special Storage Condition, Specify: Fragile. Keep away from sunlight. This way up
CLOSE

Clinically Relevant Size

[?]
Size Type Text
Device Size Text, specify: Priming Volume 150 Milliliter
CLOSE

Device Status

In Commercial Distribution
September 09, 2016

CLOSE

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
54987350705735 10 04987350705730 In Commercial Distribution
CLOSE

Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
CLOSE

Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
CLOSE

Production Identifier(s) in UDI

[?]
Yes
No
Yes
No
No CLOSE

Customer Contact

[?]
+1(800)521-2818
xx@xx.xx
CLOSE