Identity

Trade Name
Hako-Med FDA UDI
Generic Name
Interferential electrical stimulation system FDA UDI
Model / Reference
PROElecDT2000 FDA UDI

Identifiers

Primary DI / UDI-DI
04260653010016 FDA UDI
FDA Product Code
LIH FDA UDI
IPF FDA UDI
GMDN Term
Interferential electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
890.5850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Interferential electrical stimulation system

Hako-Med by HAKO-MED Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Interferential electrical stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c3bdb36a-c375-4983-93e1-9f030685fc57 32 fields · synced May 30, 2026