Primary Device ID | 08592346855236 |
NIH Device Record Key | 1e81eb58-cd35-4a03-b6fc-4318a0f78fca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MediVitop |
Version Model Number | MT25 O2 3/4UNF CGA540 DS S |
Catalog Number | 0712600US |
Company DUNS | 819753190 |
Company Name | GCE, s.r.o. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
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 | 08592346855236 [Primary] |
CAN | Regulator, Pressure, Gas Cylinder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-07 |
Device Publish Date | 2022-11-29 |
08592346855236 | The regulator acts as a pressure-reducer, gas from the cylinder valve passes through the pressur |
08592346898165 | The regulator acts as a pressure-reducer, gas from the cylinder valve passes through the pressur |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MEDIVITOP 87200452 5353298 Live/Registered |
GCE Holding AB 2016-10-12 |