Primary Device ID | 00628101609245 |
NIH Device Record Key | ee5023bc-7d39-4b7e-b8af-4dff8a3c93ba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgical Free Flow Vacuum Regulator |
Version Model Number | SCSA |
Company DUNS | 005192885 |
Company Name | OHIO MEDICAL, LLC |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 18478550500 |
customer.service@ohiomedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00628101609245 [Primary] |
GS1 | 08688250002252 [Previous] |
GCX | Apparatus, Suction, Operating-Room, Wall Vacuum Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-08 |
Device Publish Date | 2020-04-30 |
08688250002252 | Vacuum Regulator, Surgical Free Flow, 200mmHg Analog |
08688250002238 | Vacuum Regulator, Surgical Free Flow, 760mmHg Analog |
00628101609245 | Vacuum Regulator, Surgical Free Flow, 200mmHg Analog |
00628101609221 | Vacuum Regulator, Surgical Free Flow, 760mmHg Analog |