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Ionto Plus Medium Electrodes

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
Ionto Plus Medium Electrodes FDA UDI
Generic Name
Drug-delivery iontophoresis patch FDA UDI
Device Name
Iontophoresis Drug Delivery Medium Kit Electrodes - 2.5cc, 4mA-min incl. buffered return 3.25" x 3.25" FDA UDI
Model / Reference
201-449 FDA UDI
Description
Iontophoresis Drug Delivery Medium Kit Electrodes - 2.5cc, 4mA-min incl. buffered return 3.25" x 3.25" FDA UDI

Identifiers

Primary DI / UDI-DI
00092237901762 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

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Drug-delivery iontophoresis patch

Ionto Plus Medium Electrodes by Compass Health Brands Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Drug-delivery iontophoresis patch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Compass Health Brands Corp.

Sources (1)

  • FDA UDI a3f3527c-30bf-4248-84f6-a47b8506c662 34 fields · synced May 30, 2026