Primary Device ID | 00724995155247 |
NIH Device Record Key | c7fc7f16-625f-430c-9b91-cdb11036a55c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgigraphic |
Version Model Number | Surgigraphic 6000 Table |
Catalog Number | TA01 |
Company DUNS | 036985604 |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00724995155247 [Primary] |
GDC | TABLE, OPERATING-ROOM, ELECTRICAL |
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 |
50724995216905 - Revital-Ox | 2024-04-25 Revital-Ox PAA HLD Solution Part B is used Revital-Ox PAA HLD Part A and the enspire 300 Series Automated Endoscope Reprocessor |
50724995216929 - Revital-Ox | 2024-04-25 Revital-Ox PAA HLD Solution Part A is used Revital-Ox PAA HLD Part B and the enspire 300 Series Automated Endoscope Reprocessor |
00724995217587 - NA | 2024-04-25 enspire 300 Connector Olympus Channel Separator is used with the enspire 300 Series Automated Endoscope Reprocessor |
00724995217594 - NA | 2024-04-25 enspire 300 Connector Olympus Channel Separator is used with the enspire 300 Series Automated Endoscope Reprocessor |
00724995217600 - NA | 2024-04-25 enspire 300 Connector Olympus Air Water Valve is used with the enspire 300 Series Automated Endoscope Reprocessor |
00724995217617 - NA | 2024-04-25 enspire 300 Connector Olympus Air Water Valve is used with the enspire 300 Series Automated Endoscope Reprocessor |
00724995217624 - NA | 2024-04-25 enspire 300 Connector Olympus Suction Valve is used with the enspire 300 Series Automated Endoscope Reprocessor |
00724995217631 - NA | 2024-04-25 enspire 300 Connector Olympus Suction Valve is used with the enspire 300 Series Automated Endoscope Reprocessor |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SURGIGRAPHIC 78199011 2944883 Live/Registered |
STERIS CORPORATION 2002-12-31 |