Primary Device ID | 38033178112360 |
NIH Device Record Key | b69ec55e-70fd-4dbf-b20f-2fb7e037c93b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INSPIRE |
Version Model Number | 8 PH.I.S.I.O. |
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 | 08033178112369 [Primary] |
GS1 | 38033178112360 [Package] Contains: 08033178112369 Package: BOX [2 Units] In Commercial Distribution |
DTZ | OXYGENATOR, CARDIOPULMONARY BYPASS |
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 | 2015-05-13 |
38033178113237 | 7 DUAL |
38033178113213 | 7 |
38033178113183 | 7 M |
38033178113015 | SVR 1200 |
38033178112421 | 8F DUAL PH.I.S.I.O. |
38033178112414 | 6F DUAL PH.I.S.I.O. |
38033178112407 | 8 DUAL PH.I.S.I.O. |
38033178112391 | 6 DUAL PH.I.S.I.O. |
38033178112384 | 8F PH.I.S.I.O. |
38033178112377 | 6F PH.I.S.I.O. |
38033178112360 | 8 PH.I.S.I.O. |
38033178112353 | 6 PH.I.S.I.O. |
38033178112308 | HVR DUAL |
38033178112292 | HVR |
38033178112285 | 8F M |
38033178112278 | 6F M |
38033178112261 | 8M |
38033178112254 | 6M |
38033178113367 | 7F DUAL |
38033178113350 | 7F |
38033178113343 | 7F M |
08033178112994 | Bracket |
08033178112987 | Bracket 1200 |
08033178112970 | Bracket |
08033178111966 | Bracket |
08033178111959 | Bracket |