Primary Device ID | 30190302004422 |
NIH Device Record Key | 319d4afb-a6a3-41d3-ad7b-a4f05242e6fd |
Commercial Distribution Discontinuation | 2020-04-20 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | GlutaMAX™-I (100X) |
Version Model Number | 35050061 |
Company DUNS | 118793157 |
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 | 10190302004428 [Primary] |
GS1 | 30190302004422 [Package] Contains: 10190302004428 Package: Case [20 Units] Discontinued: 2020-04-17 Not in Commercial Distribution |
KIT | MEDIA AND COMPONENTS, SYNTHETIC CELL AND TISSUE CULTURE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-12 |
Device Publish Date | 2016-08-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GLUTAMAX 97104186 not registered Live/Pending |
Life Technologies Corporation 2021-11-02 |
GLUTAMAX 79061516 3651456 Dead/Cancelled |
ISTITUTO PROFILATTICO E FARMACEUTICO CANDIOLI E C. S.R.L. (also known as CANDIOLI FARMACEUTICI S.R.L.) 2008-09-24 |
GLUTAMAX 75716569 not registered Dead/Abandoned |
MAXI HEALTH RESEARCH INC. 1999-05-27 |
GLUTAMAX 74622539 1938883 Live/Registered |
TD BANK, N.A. 1995-01-18 |