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Interlink

FDA UDI

Class II (US FDA UDI)

by Baxter International Inc.

Identity

Trade Name
INTERLINK FDA UDI
Generic Name
Blood transfusion set, non-exchange FDA UDI
Device Name
Y-Type Blood/Solution Set with 40 and 150 Micron Dual Screen Filter and Pressure Pump, Injection Site, Male Luer Lock Adapter with Retractable Collar FDA UDI
Model / Reference
4C6839 FDA UDI
Description
Y-Type Blood/Solution Set with 40 and 150 Micron Dual Screen Filter and Pressure Pump, Injection Site, Male Luer Lock Adapter with Retractable Collar FDA UDI

Identifiers

Catalog Number
4C6839 FDA UDI
Primary DI / UDI-DI
00085412065298 FDA UDI
FDA Product Code
FPB FDA UDI
FPA FDA UDI
GMDN Term
Blood transfusion set, non-exchange FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8216e18b-98fc-4d84-a5fe-38185617849a 36 fields · synced May 30, 2026