RPMI Medium 1640

GUDID 10190302004893

LIFE TECHNOLOGIES CORPORATION

Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD
Primary Device ID10190302004893
NIH Device Record Key997193c0-5f0d-4dc6-b6fc-ad3cee1c5f1e
Commercial Distribution Discontinuation2022-05-25
Commercial Distribution StatusNot in Commercial Distribution
Brand NameRPMI Medium 1640
Version Model Number61870150
Company DUNS118793157
Company NameLIFE TECHNOLOGIES CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110190302004893 [Primary]

FDA Product Code

KITMEDIA AND COMPONENTS, SYNTHETIC CELL AND TISSUE CULTURE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-05-26
Device Publish Date2016-08-01

On-Brand Devices [RPMI Medium 1640]

1019030200421331800105
1019030200419031800022
1019030200384123400062
1019030200383423400021
1019030200420631800089
1019030200201111875176
1019030200200411875168
3019030200199511875085
3019030200198811875101
3019030200197111875093
3019030200376022400071
3019030200375322400089
1019030200374222400097
1019030200503672400153
1019030200502972400146
3019030200501672400047
1019030200489361870150
1019030200488661870143
3019030200487361870036
3019030200359321870084
3019030200358621870076

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