Rapidfill

FDA UDI

Class II (US FDA UDI)

by Baxter Healthcare Corp

Identity

Trade Name: RAPIDFILL FDA UDI
Generic Name: Fluid transfer set, general-purpose FDA UDI
Device Name: Connector, Luer Lock-to-Luer Lock FDA UDI
Model / Reference: H93813901 FDA UDI
Description: Connector, Luer Lock-to-Luer Lock FDA UDI

Identifiers

Catalog Number: H93813901 FDA UDI
Primary DI / UDI-DI: 00085412478364 FDA UDI
510(k) Number: K872743 FDA UDI
FDA Product Code: FMF FDA UDI
GMDN Term: Fluid transfer set, general-purpose FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5860 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Fluid transfer set, general-purpose

Rapidfill by Baxter Healthcare Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K872743 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Baxter Healthcare Corp

Sources (1)

FDA UDI f76b7303-f0d6-4164-b311-5365627543ad 36 fields · synced May 30, 2026