Primary Device ID | 34987350706493 |
NIH Device Record Key | 27209e62-0cfa-436f-bfd7-f5bdee48f2ca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CAPIOX® VENOUS RESERVOIR |
Version Model Number | CX*VRA0401T2 |
Company DUNS | 690543319 |
Company Name | TERUMO CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-800-521-2818 |
cvscustomerservice@terumomedical.com |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. This way up. Keep away from sunlight. Keep away from rain. |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. This way up. Keep away from sunlight. Keep away from rain. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04987350706492 [Primary] |
GS1 | 34987350706493 [Package] Contains: 04987350706492 Package: [4 Units] In Commercial Distribution |
DTM | Filter, Blood, Cardiopulmonary Bypass, Arterial Line |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-01-22 |
Device Publish Date | 2015-09-15 |
34987350706691 | CX*VRA1001T2 |
34987350706592 | CX*VRA0701T2 |
34987350706493 | CX*VRA0401T2 |
34987350706394 | CX*VRA0101T2 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CAPIOX 74561748 1957236 Live/Registered |
TERUMO KABUSHIKI KAISHA 1994-08-16 |
CAPIOX 73401694 1295899 Dead/Cancelled |
Terumo Kabushiki Kaisha 1982-11-04 |