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Ionto Plus Large, Box of 12

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
Ionto Plus Large, Box of 12 FDA UDI
Generic Name
Drug-delivery iontophoresis patch FDA UDI
Device Name
Iontophoresis Drug Delivery Electrodes FDA UDI
Model / Reference
201-453 FDA UDI
Description
Iontophoresis Drug Delivery Electrodes FDA UDI

Identifiers

Primary DI / UDI-DI
10853904006039 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
Not 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Ionto Plus Large, Box of 12 by Compass Health Brands Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bf0ded30-7306-447a-8d8e-444b7012cddf 35 fields · synced May 31, 2026