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Interlink

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
Interlink FDA UDI
Generic Name
Luer/Luer linear connector, single-use FDA UDI
Device Name
Blunt Plastic Cannula FDA UDI
Model / Reference
303345 FDA UDI
Description
Blunt Plastic Cannula FDA UDI

Identifiers

Catalog Number
303345 FDA UDI
Primary DI / UDI-DI
00382903033454 FDA UDI
510(k) Number
K974363 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Luer/Luer linear connector, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luer/Luer linear connector, single-useLuer-formatted bag access spike

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

Similar devices

Also classified as Luer-formatted bag access spike.

Cleared under the same submission

K974363 also covers:

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 47e3ed2a-9f00-48ca-9e2d-cbecea4752f3 36 fields · synced May 30, 2026