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Horizon

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
Horizon FDA UDI
Generic Name
CD56 neural cell adhesion molecule-1 (NCAM-1) IVD, antibody FDA UDI
Device Name
BD Horizon™ CD56 (NCAM16.2) BV605 FDA UDI
Model / Reference
663990 FDA UDI
Description
BD Horizon™ CD56 (NCAM16.2) BV605 FDA UDI

Identifiers

Catalog Number
663990 FDA UDI
Primary DI / UDI-DI
00382906639905 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
CD56 neural cell adhesion molecule-1 (NCAM-1) IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Category: CD56 neural cell adhesion molecule-1 (NCAM-1) IVD, antibody

Horizon by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CD56 neural cell adhesion molecule-1 (NCAM-1) IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a9cddc7e-2db8-4c14-ab67-8c2d5fdc107f 36 fields · synced May 30, 2026