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Curlin

FDA UDI

Class II (US FDA UDI)

by Zevex International, Inc.

Identity

Trade Name
Curlin FDA UDI
Generic Name
Portable/mobile rechargeable battery pack FDA UDI
Device Name
Curlin 6000 Lithium Ion Battery Pack FDA UDI
Model / Reference
Battery Pack FDA UDI
Description
Curlin 6000 Lithium Ion Battery Pack FDA UDI

Identifiers

Catalog Number
360-2030 FDA UDI
Primary DI / UDI-DI
10814844001003 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Portable/mobile rechargeable battery pack 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Portable/mobile rechargeable battery pack

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

Similar devices

Also classified as Portable/mobile rechargeable battery pack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6c10b726-dc84-44b2-87da-0d13a5719ad7 35 fields · synced Jun 8, 2026