Primary Device ID | 38033178113107 |
NIH Device Record Key | 01304f2e-19c6-4b28-a02b-6f7c54ec63c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | B-CAPTA |
Version Model Number | 3/8" VENOUS CUVETTE |
Company DUNS | 442126587 |
Company Name | SORIN GROUP ITALIA SRL |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08033178113106 [Primary] |
GS1 | 38033178113107 [Package] Contains: 08033178113106 Package: BOX [10 Units] In Commercial Distribution |
DRY | MONITOR, BLOOD-GAS, ON-LINE, CARDIOPULMONARY BYPASS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-13 |
Device Publish Date | 2021-05-05 |
38033178113527 | 3/8" ARTERIAL CUVETTE |
38033178113510 | 1/4" ARTERIAL CUVETTE |
38033178113114 | 1/2" VENOUS CUVETTE |
38033178113107 | 3/8" VENOUS CUVETTE |
38033178113091 | 1/4" VENOUS CUVETTE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
B-CAPTA 79240105 5724415 Live/Registered |
SORIN GROUP ITALIA S.R.L. 2018-06-28 |