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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 Extension Set with 1.2 Micron Downstream Filter, Air Eliminating Filter, INTERLINK Injection Site FDA UDI
Model / Reference
2C1103 FDA UDI
Description
Non-DEHP Extension Set with 1.2 Micron Downstream Filter, Air Eliminating Filter, INTERLINK Injection Site FDA UDI

Identifiers

Catalog Number
2C1103 FDA UDI
Primary DI / UDI-DI
00085412000503 FDA UDI
510(k) Number
K952074 FDA UDI
FDA Product Code
FPA 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

K952074 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 2cb21490-1c0f-4fbc-8456-21a48f808ce0 36 fields · synced May 31, 2026