Primary Device ID | 10190302000536 |
NIH Device Record Key | ad078129-a7c9-4407-8ff6-60a95d435289 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Veriti™ Dx 384-Well Thermal Cycler |
Version Model Number | 9913 |
Company DUNS | 628548377 |
Company Name | LIFE TECHNOLOGIES HOLDINGS PTE. LTD. |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10190302000536 [Primary] |
OUL | Thermocycler, generic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-07-07 |
Device Publish Date | 2016-08-01 |
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10190302019231 - KingFisher™ Apex Dx Purification Instrument | 2023-08-11 |
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10190302019255 - KingFisher™ Apex Dx 96 Combi Head | 2023-08-11 |
10190302019262 - KingFisher™ Apex Dx 96 Deep Well Head | 2023-08-11 |
10190302019279 - KingFisher™ Apex Dx 24 Combi Head | 2023-08-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() VERITI 97454915 not registered Live/Pending |
Veriti Security Inc. 2022-06-13 |
![]() VERITI 78946610 3486513 Live/Registered |
Applied Biosystems, LLC. 2006-08-07 |