Primary Device ID | 00724995094850 |
NIH Device Record Key | 178e6bcc-bdc1-499e-ac1f-d4b9f7433ff6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Revital-Ox |
Version Model Number | 2D94Q0 |
Catalog Number | 2D94Q0 |
Company DUNS | 139424188 |
Company Name | STERIS CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | +1(800)548-4873 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00724995094850 [Primary] |
FFY | Adaptor, bulbs, miscellaneous, for endoscope |
PHT | Basin for endoscope reprocessing |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-04-08 |
Device Publish Date | 2021-03-31 |
00724995094850 | Revital-Ox Flexible Container Round is for the transport or soaking of rigid endoscopes. |
00724995094843 | Revital-Ox Rigid Container System is for the transport or soaking of rigid endoscopes and access |
50724995216929 | Revital-Ox PAA HLD Solution Part A is used Revital-Ox PAA HLD Part B and the enspire 300 Series |
50724995216905 | Revital-Ox PAA HLD Solution Part B is used Revital-Ox PAA HLD Part A and the enspire 300 Series |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() REVITAL-OX 97113616 not registered Live/Pending |
STERIS Corporation 2021-11-08 |
![]() REVITAL-OX 85526241 4400911 Live/Registered |
STERIS CORPORATION 2012-01-26 |
![]() REVITAL-OX 85337306 4283577 Live/Registered |
STERIS CORPORATION 2011-06-03 |