← Back to catalogue

Interlink

FDA UDI

Class II (US FDA UDI)

by Baxter International Inc.

Identity

Trade Name
INTERLINK FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
Non-DEHP I.V. Connector Loop, Injection Site, Male Luer Lock with Rotating Collar FDA UDI
Model / Reference
2N3373 FDA UDI
Description
Non-DEHP I.V. Connector Loop, Injection Site, Male Luer Lock with Rotating Collar FDA UDI

Identifiers

Catalog Number
2N3373 FDA UDI
Primary DI / UDI-DI
00085412004891 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Basic intravenous administration set, noninvasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic intravenous administration set, noninvasive

Interlink by Baxter International Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Baxter International Inc.

Sources (1)

  • FDA UDI 61083dbb-26f4-470f-b4ed-26c1a6d37453 35 fields · synced Jun 1, 2026