DHI Media & Controls 10-120100

GUDID 30014613331117

HBSS, NO CA, NO MG

DIAGNOSTIC HYBRIDS, INC.

Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD
Primary Device ID30014613331117
NIH Device Record Key0f41665e-ff3a-494e-a9bf-b5b16a7f783e
Commercial Distribution StatusIn Commercial Distribution
Brand NameDHI Media & Controls
Version Model Number10-120100
Catalog Number10-120100
Company DUNS117359612
Company NameDIAGNOSTIC HYBRIDS, INC.
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com
Phone+1(858)552-1100
Emailtechnicalsupport@quidel.com

Device Identifiers

Device Issuing AgencyDevice ID
GS130014613331117 [Primary]

FDA Product Code

KIPFORMULATIONS, BALANCED SALT SOLUTIONS

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-29
Device Publish Date2018-09-26

On-Brand Devices [DHI Media & Controls]

30014613331353REFEED MEDIUM ZERO-SERUM-3AB
30014613331346ZERO-SERUM REFEED MEDIUM-PSGA
30014613331339SUPER E-MIX REFEED MEDIUM
30014613331322SUPER E-MIX REFEED MEDIUM
30014613331315REFEED MEDIUM ZERO-SERUM-PS
30014613331308REFEED MEDIUM ZERO-SERUM-PS
30014613331292REFEED MEDIUM 10%FBS
30014613331285REFEED MEDIUM 10%FBS
30014613331278CTISOLATION MEDIUM
30014613331261REFEED MEDIUM RMIX 03T
30014613331254REFEED MEDIUM RMIX 03T
30014613331223REFEED MEDIUM 01
30014613331216CMV TURBOTREAT MEDIUM
30014613331186MRC-5 GROWTH MEDIUM
30014613331179PLANTING MEDIUM BASE
30014613331162SUPPL FOR 10-200100 EU2 PLT MD
30014613331155STANDARD PLANTING MEDIUM
30014613331148REFEED MEDIUM 5% 500ML BTL
30014613331131DMEM, 10% FBS, 1000 ML
30014613331124HBSS, NO CA, NO MG
30014613331117HBSS, NO CA, NO MG
30014613331100TRYPSIN CONC, 7ML IN PBS
30014613331094TRYPSIN-EDTA
30014613331087PBS 10X
30014613331070HBSS DILUENT
30014613331063HBSS DILUENT
30014613331056ANTIBIOTIC SOLUTION
30014613331049GENTAMICIN 50 MG/ML
30014613331032AMPHOTERICIN B, 250 UG/ML
30014613331025PEN/STREP 10K/10K
30014613330998C. DIFFICILE ANTI-TOXIN REAGENT
30014613330981C. DIFFICILE TOXIN Control
30014613330974C. DIFFICILE SPEC. DILUENT
30014613330967C. DIFFICILE TOXIN DETECTION

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.