Primary Device ID | 00812345029901 |
NIH Device Record Key | 76608927-915b-46ac-b2df-c93c37b07b77 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Quik-Prep |
Version Model Number | 011440-004 |
Company DUNS | 062046149 |
Company Name | MORTARA INSTRUMENT, 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 | 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 | true |
OTC Over-The-Counter | false |
Phone | 888-667-8272 |
techsupport@mortara.com | |
Phone | 888-667-8272 |
techsupport@mortara.com |
Storage Environment Temperature | Between 0 Degrees Fahrenheit and 185 Degrees Fahrenheit |
Storage Environment Temperature | Between 0 Degrees Fahrenheit and 185 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812345029901 [Primary] |
DRX | Electrode, Electrocardiograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-06-29 |
Device Publish Date | 2016-09-24 |
00812345029901 | Electrode application system |
00812345022780 | Electrode application system |
21081234502474 | Electrodes |
21081234502471 | Electrodes |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
QUIK-PREP 78449677 not registered Dead/Abandoned |
Quikrete International, Inc. 2004-07-13 |
QUIK-PREP 78439344 3022115 Live/Registered |
General Cable Technologies Corporation 2004-06-22 |
QUIK-PREP 73390045 1274743 Dead/Cancelled |
Lifton; Lester J. 1982-09-27 |
QUIK-PREP 73310353 1214755 Dead/Cancelled |
Quinton Instrument Co. 1981-05-14 |