Iontophoresis Dupel Blue Medium - Standard 2.5 mL

FDA UDI

Class II (US FDA UDI)

by Empi

Identity

Trade Name: Iontophoresis Dupel Blue Medium - Standard 2.5 mL FDA UDI
Generic Name: Drug-delivery iontophoresis patch FDA UDI
Model / Reference: 199335-001 FDA UDI

Identifiers

Primary DI / UDI-DI: 00888912151351 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

Iontophoresis Dupel Blue Medium - Standard 2.5 mL by Empi — 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: Empi

Sources (1)

FDA UDI 4560f868-2195-478e-a1dd-55d9f94db3aa 32 fields · synced May 30, 2026