Repeater

FDA UDI

Class II (US FDA UDI)

by Baxter Healthcare Corp

Identity

Trade Name: REPEATER FDA UDI
Generic Name: Intravenous solution compounder FDA UDI
Device Name: REPEATER Pump, Refurbished Fluid Transfer Pump FDA UDI
Model / Reference: H938099ER FDA UDI
Description: REPEATER Pump, Refurbished Fluid Transfer Pump FDA UDI

Identifiers

Catalog Number: H938099ER FDA UDI
Primary DI / UDI-DI: 00085412482514 FDA UDI
FDA Product Code: NEP FDA UDI
GMDN Term: Intravenous solution compounder 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

FDA UDI

Single Use

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

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intravenous solution compounder

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

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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 0c1a62f8-3ec7-434b-bbba-8053f9e8a30b 36 fields · synced May 30, 2026