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BD Intelliport System

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Intelliport System FDA UDI
Generic Name
Intravenous injection automated detection/documentation system processor/transmitter FDA UDI
Device Name
SYRINGE LABELER FDA UDI
Model / Reference
516800 FDA UDI
Description
SYRINGE LABELER FDA UDI

Identifiers

Catalog Number
516800 FDA UDI
Primary DI / UDI-DI
00382905168000 FDA UDI
FDA Product Code
PCH FDA UDI
FPA FDA UDI
GMDN Term
Intravenous injection automated detection/documentation system processor/transmitter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3990 FDA UDI
880.5440 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Intravenous injection automated detection/documentation system processor/transmitter

BD Intelliport System by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous injection automated detection/documentation system processor/transmitter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI 98c5e125-3574-4431-ad7d-5240df32a762 34 fields · synced May 30, 2026