ActivaPatch IontoGo 12.0

FDA UDI

Class II (US FDA UDI)

by Activatek Inc.

Identity

Trade Name: ActivaPatch IontoGo 12.0 FDA UDI
Generic Name: Drug-delivery iontophoresis patch FDA UDI
Device Name: ActivaPatch IontoGo 12.0 carton with 6 pouches, 12 hour iontophoresis delivery FDA UDI
Model / Reference: 001-90 FDA UDI
Description: ActivaPatch IontoGo 12.0 carton with 6 pouches, 12 hour iontophoresis delivery FDA UDI

Identifiers

Catalog Number: NC89191 FDA UDI
Primary DI / UDI-DI: 00859975005226 FDA UDI
FDA Product Code: EGJ FDA UDI
GMDN Term: Drug-delivery iontophoresis patch 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

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Drug-delivery iontophoresis patch

ActivaPatch IontoGo 12.0 by Activatek Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Ionto Plus Butterfly — COMPASS HEALTH BRANDS CORP. · Class II

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: Activatek Inc.

Sources (1)

FDA UDI 3b8f9cdd-1b9f-4701-9d80-5a6ff7cca482 34 fields · synced May 30, 2026