Primary Device ID | 00677964022340 |
NIH Device Record Key | 3eae6036-a724-4c4a-aaa5-308574e7a6ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FiberFlo |
Version Model Number | 93022-083 |
Company DUNS | 068199363 |
Company Name | MEDIVATORS INC. |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00677964022340 [Primary] |
FIP | Subsystem, Water Purification |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2018-01-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FIBERFLO 88151899 not registered Live/Pending |
Comfort DTC, Inc. 2018-10-11 |
FIBERFLO 78539951 3070566 Live/Registered |
MAR COR PURIFICATION, INC. 2004-12-30 |
FIBERFLO 78191063 3291444 Dead/Cancelled |
Solomon Grind-Chem Service, Inc. 2002-12-04 |
FIBERFLO 76174137 2575663 Dead/Cancelled |
Beyond, Inc. 2000-12-04 |
FIBERFLO 74287092 1761229 Live/Registered |
MAR COR PURIFICATION, INC. 1992-06-22 |
FIBERFLO 74287092 1761229 Live/Registered |
EVOQUA WATER TECHNOLOGIES LTD 1992-06-22 |
FIBERFLO 73120793 1091867 Live/Registered |
KOMBI LTD. 1977-03-29 |