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Curlin IV Pump System

FDA UDI

Class II (US FDA UDI)

by Zevex International, Inc.

Identity

Trade Name
Curlin IV Pump System FDA UDI
Generic Name
Patient-controlled analgesia infusion pump FDA UDI
Device Name
Curlin IV Pump System FDA UDI
Model / Reference
Curlin Pump FDA UDI
Description
Curlin IV Pump System FDA UDI

Identifiers

Primary DI / UDI-DI
10814844000365 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient-controlled analgesia infusion pump

Curlin IV Pump System by Zevex International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient-controlled analgesia infusion pump.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2c9e097f-4b7c-4312-822c-e7f1e06a41a6 34 fields · synced May 30, 2026