Primary Device ID | 00849832002079 |
NIH Device Record Key | 5636397a-67a5-42cd-937a-e93161c0bf46 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ThermoBrite |
Version Model Number | 3800-004852-001 |
Company DUNS | 082930884 |
Company Name | Leica Biosystems Richmond, Inc. |
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 | false |
Phone | +1(844)534-2262 |
tech.support@Leicabiosystems.com |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 * |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00849832002079 [Primary] |
JRG | BLOCK, HEATING |
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 | 2017-09-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
THERMOBRITE 76578783 2999949 Live/Registered |
LEICA BIOSYSTEMS RICHMOND, INC. 2004-03-01 |
THERMOBRITE 73719143 not registered Dead/Abandoned |
HARSHAW/FILTROL PARTNERSHIP 1988-03-28 |