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Interlink

FDA UDI

Class II (US FDA UDI)

by Baxter International Inc.

Identity

Trade Name
INTERLINK FDA UDI
Generic Name
Intravenous line filter FDA UDI
Device Name
Non-DEHP Minivolume Extension Set, Injection Site, 0.2 Micron Downstream Filter, Male Luer Lock Adapter FDA UDI
Model / Reference
1C8740 FDA UDI
Description
Non-DEHP Minivolume Extension Set, Injection Site, 0.2 Micron Downstream Filter, Male Luer Lock Adapter FDA UDI

Identifiers

Catalog Number
1C8740 FDA UDI
Primary DI / UDI-DI
00085412082028 FDA UDI
510(k) Number
K113227 FDA UDI
FDA Product Code
FPB FDA UDI
GMDN Term
Intravenous line filter 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: Intravenous line filter

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

Similar devices

Also classified as Intravenous line filter.

Cleared under the same submission

K113227 also covers:

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 a4eb4294-bc81-4b7e-818d-26478a99984d 36 fields · synced May 30, 2026