DHI Media & Controls 03-05050

GUDID 30014613330974

C. DIFFICILE SPEC. DILUENT

DIAGNOSTIC HYBRIDS, INC.

Cell culture medium IVD

• Primary Device ID: 30014613330974
• NIH Device Record Key: e934a160-683d-49a3-a254-114417e8a2eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DHI Media & Controls
• Version Model Number: 03-05050
• Catalog Number: 03-05050
• Company DUNS: 117359612
• Company Name: DIAGNOSTIC HYBRIDS, INC.
• 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: true
• Device Combination Product: false
• Single Use: true
• 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

Customer Support Contacts

• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	30014613330974 [Primary]

FDA Product Code

• KIP: FORMULATIONS, BALANCED SALT SOLUTIONS

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-29
• Device Publish Date: 2018-09-26

On-Brand Devices [DHI Media & Controls]

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