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BD BBL™ Streptocard™ Enzyme Latex Test Kit

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 240918

by Becton Dickinson And Company

Identity

Trade Name
BBL Streptocard EUDAMED
BD BBL™ Streptocard™ Enzyme Latex Test Kit FDA UDI
Generic Name
Beta-haemolytic Streptococcus serological grouping IVD, kit, agglutination FDA UDI
Device Name
BD BBL™ Streptocard™ Enzyme Latex Test Kit EUDAMED
BD BBL™ Streptocard™ Enzyme Latex Test Kit, 50 Tests FDA UDI
Model / Reference
240918 EUDAMEDFDA UDI
Description
BD BBL™ Streptocard™ Enzyme Latex Test Kit, 50 Tests FDA UDI

Identifiers

Catalog Number
240918 FDA UDI
Primary DI / UDI-DI
00382902409182 EUDAMEDFDA UDI
Basic UDI-DI
038290MPOMLCHHF6 EUDAMED
FDA Product Code
GTZ FDA UDI
EMDN Code
W0105011199 STREPTOCOCCAL REAGENTS - OTHER EUDAMED
GMDN Term
Beta-haemolytic Streptococcus serological grouping IVD, kit, agglutination FDA UDI

Classification

Device Class
Class B EUDAMED
Class I FDA UDI
Regulation Number
866.3740 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

Yes

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 — 39.5 Milliliter FDA UDI

Category: Beta-haemolytic Streptococcus serological grouping IVD, kit, agglutination

BD BBL™ Streptocard™ Enzyme Latex Test Kit by Becton Dickinson And Company — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Beta-haemolytic Streptococcus serological grouping IVD, kit, agglutination.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 074c006b-dec9-4ea0-9a7d-bb4b70bd60af 37 fields · synced Jun 19, 2026
  • EUDAMED 8d6a6b01-81fc-4c44-ac30-93e6534f06a8 61 fields · synced Jun 19, 2026