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Bbl

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 296182

by Becton, Dickinson and Company

Identity

Trade Name
BBL EUDAMED
BD BBL™ Sabouraud Dextrose Agar Deeps FDA UDI
Generic Name
Differential/selective agar culture medium IVD FDA UDI
Device Name
BD BBL™ Sabouraud Dextrose Agar Slants, 10 size A tubes, BD BBL™ Sabouraud Dextrose Agar Slants, 100 size A tubes, BD BBL™ SabouraudDextrose Agar with Chloramphenicol Slants and BD BBL™ SabouraudDextrose Agar Deeps EUDAMED
BD BBL™ Sabouraud Dextrose Agar Deeps, 20 mL, Carton of 100 size A tubes FDA UDI
Model / Reference
296182 EUDAMEDFDA UDI
Description
BD BBL™ Sabouraud Dextrose Agar Deeps, 20 mL, Carton of 100 size A tubes FDA UDI

Identifiers

Catalog Number
296182 FDA UDI
Primary DI / UDI-DI
30382902961827 EUDAMEDFDA UDI
Basic UDI-DI
038290JQNNEXCEEX EUDAMED
Unit of Use DI
00382902961826 EUDAMED
FDA Product Code
KZI FDA UDI
EMDN Code
W0104010206 MEDIA IN TUBES (SOLID & LIQUID) EUDAMED
GMDN Term
Differential/selective agar culture medium IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
866.2330 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 20 Milliliter FDA UDI

Bbl by Becton, Dickinson and Company — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000018910
Authorised Representative
Becton Dickinson Ireland Limited IE-AR-000007610

Sources (2)

  • EUDAMED 846f2647-c1c5-4f23-a97d-a52e9437b927 61 fields · synced Oct 6, 2026
  • FDA UDI 11a13fef-9723-4873-a2a9-8497e3ee72a9 37 fields · synced May 29, 2026