Primary Device ID | 38033178000063 |
NIH Device Record Key | 4e0bbcac-c755-407c-93ec-377a0f25f6d3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Venous Cannula |
Version Model Number | V122-24 |
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 | 08033178000062 [Primary] |
GS1 | 38033178000063 [Package] Contains: 08033178000062 Package: BOX [10 Units] In Commercial Distribution |
DWF | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2022-08-05 |
Device Publish Date | 2016-03-21 |
38033178000247 | V112-50 |
38033178000230 | V112-40 |
38033178000223 | V112-32 |
38033178000179 | V152-36 |
38033178000162 | V152-32 |
38033178000100 | V122-36 |
38033178000094 | V122-34 |
38033178000087 | V122-32 |
38033178000070 | V122-28 |
38033178000063 | V122-24 |
38033178000056 | V122-22 |
38033178000049 | V122-20 |
38033178000032 | V122-18 |
38033178000025 | V122-16 |
38033178000018 | V122-14 |