Daavlin

FDA UDI

Class II (US FDA UDI)

by Hidrex GmbH

Identity

Trade Name: DAAVLIN FDA UDI
Generic Name: Hyperhidrosis iontophoresis system FDA UDI
Device Name: Daavlin Aquex Tap Water Iontophoresis Device FDA UDI
Model / Reference: Aquex (DAAV1000) FDA UDI
Description: Daavlin Aquex Tap Water Iontophoresis Device FDA UDI

Identifiers

Catalog Number: DAAV16110 FDA UDI
Primary DI / UDI-DI: 04250571300818 FDA UDI
FDA Product Code: EGJ FDA UDI
GMDN Term: Hyperhidrosis iontophoresis system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5525 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

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

FDA UDI

Category: Hyperhidrosis iontophoresis system

Daavlin by Hidrex GmbH — 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: Hidrex GmbH

Sources (1)

FDA UDI ca6cc34a-8fa4-4c64-b406-2fc29c36850c 35 fields · synced Jun 1, 2026