Curlin

FDA UDI

Class II (US FDA UDI)

by Zevex International, Inc.

Identity

Trade Name: Curlin FDA UDI
Generic Name: Patient-controlled analgesia infusion pump FDA UDI
Device Name: Curlin Bolus Cord FDA UDI
Model / Reference: Curlin Bolus Cord FDA UDI
Description: Curlin Bolus Cord FDA UDI

Identifiers

Catalog Number: 56872 FDA UDI
Primary DI / UDI-DI: 10814844001010 FDA UDI
FDA Product Code: FRN FDA UDI
GMDN Term: Patient-controlled analgesia infusion pump FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5725 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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Patient-controlled analgesia infusion pump

Curlin by Zevex International, Inc. — 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: Zevex International, Inc.

Sources (1)

FDA UDI d31c8059-1c1a-4f3d-83c2-5ab409f9c35d 35 fields · synced May 29, 2026