Water for Injection, USP Sterile Grade WFI-USP-2XL

GUDID B891WFIUSP2XL0

INTERMOUNTAIN LIFE SCIENCES, LLC

Ex vivo cell culture medium
Primary Device IDB891WFIUSP2XL0
NIH Device Record Key0f9f54e3-07df-42ac-8c27-aa1daa1c0b21
Commercial Distribution StatusIn Commercial Distribution
Brand NameWater for Injection, USP Sterile Grade
Version Model Number04
Catalog NumberWFI-USP-2XL
Company DUNS117437522
Company NameINTERMOUNTAIN LIFE SCIENCES, LLC
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com
Phone8012828610
Emailinfo@ilsgmp.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB891WFIUSP2XL0 [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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-24
Device Publish Date2020-08-14

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