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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
Solution Set, Injection Site, 15 Micron Disc Filter, Male Luer Lock Adapter FDA UDI
Model / Reference
1W5000 FDA UDI
Description
Solution Set, Injection Site, 15 Micron Disc Filter, Male Luer Lock Adapter FDA UDI

Identifiers

Catalog Number
1W5000 FDA UDI
Primary DI / UDI-DI
00085412015477 FDA UDI
510(k) Number
K870940 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

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Manufacturer

Manufacturer
Baxter International Inc.

Sources (1)

  • FDA UDI aec90fec-0126-4779-9b54-6f01e3dc6f2e 36 fields · synced May 30, 2026