Primary Device ID | 10190302006149 |
NIH Device Record Key | 526fd7c0-48d5-4f35-b337-056d37155d2c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ion PGM™ Dx Sequencing Supplies |
Version Model Number | A18936 |
Company DUNS | 080131636 |
Company Name | LIFE TECHNOLOGIES CORPORATION |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 10190302006149 [Primary] |
PFT | Reagents for molecular diagnostic test systems |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-01-22 |
Device Publish Date | 2017-04-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ION PGM 86877458 not registered Live/Pending |
Life Technologies Corporation 2016-01-15 |
ION PGM 86877413 not registered Dead/Abandoned |
Life Technologies Corporation 2016-01-15 |
ION PGM 86089872 4586079 Live/Registered |
Life Technologies Corporation 2013-10-11 |