FDA Registration Active 🇺🇸 United States

BD BBL™ Sabouraud Dextrose Agar, Emmons (Deep Fill)

Reg #: 1119779 · FEI: 1119779 · Expires 2025
Products
1
Proprietary Names
23
Establishment Types
2
Classifications
1

Registration Details

Registration Name
BECTON, DICKINSON & CO.
Registration Number
1119779
FEI Number
1119779
Status
Active
Expiry Year
2025
Initial Importer
Yes
Address
7 LOVETON CIR.
City
SPARKS
State
MD
ZIP
21152
Country
US

Owner / Operator

Firm Name
Becton Dickinson and Company
Operator Number
9922032
Address
One Becton Drive
City
Franklin Lakes
State
NJ
Postal Code
07417
Country
US

Products

Device Name Product Code
Culture Media, Enriched KZI

Proprietary Names

BD BBL™ Sabouraud Dextrose Agar, Emmons (Deep Fill) BD BBL™ Columbia Agar with 5% Sheep Blood BD BBL™ BCYE Agar BD BBL Sabouraud Brain Heart Infusion Agar Deep Fill BD BBL Trypticase Soy Agar with 10% Sheep Blood (TSA II) BD BBL Lowenstein-Jensen Medium Mycoflask BD BBL™ Brain Heart Infusion Agar with 10% Sheep Blood Deep Fill, Brain Heart Infusion Agar with 5% Sheep Blood Slants BD BBL Potato Dextrose Agar Deep Fill, Potato Flakes Agar, Potato Flakes Agar Slants with Chloramphenicol and Getamicin BD BBL Trypticase Soy Agar with 5% Horse Blood (TSA II), Trypticase Soy Agar with 5% Rabbit Blood (TSA II) BD BBL™ Brucella Agar with 5% Horse Blood BD BBL™ Cooked Meat Medium BD BBL™ Columbia Anaerobe 5% Sheep Blood Agar BD BBL Corn Meal Agar with Polysorbate 80 Deep Fill BD BBL CTA Medium with Arabinose, CTA Medium with Fructose, CTA Medium with Xylose BBL A-7 Agar, Modified, Brain Heart Infusion Agar Deep Fill, Brucella Broth BD BBL Sabouraud Dextrose Agar Emmons Mycoflask, Sabouraud Dextrose Emmons Plate BD BBL™ GN Broth BD BBL™ Sabouraud Dextrose Agar Deeps BD BBL™ Sabouraud Brain Heart Infusion Agar Slants BD BBL™ Cooked Meat Medium with Glucose, Hemin and Vitamin K1 BD BBL™ Trichosel™ Broth, Modified, with 5% Horse Serum BD BBL™ Lowenstein-Jensen Medium Slants BD BBL™ Brucella Agar with 5% Sheep Blood, Hemin and Vitamin K1

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device