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ActiPatch

FDA UDI

Class II (US FDA UDI)

by Bioelectronics Corporation

Identity

Trade Name
ActiPatch FDA UDI
Generic Name
Hand-held deep-tissue electromagnetic stimulator FDA UDI
Device Name
ActiPatch Muscle and Joint Pain Therapy Kit 5 pack FDA UDI
Model / Reference
088 FDA UDI
Description
ActiPatch Muscle and Joint Pain Therapy Kit 5 pack FDA UDI

Identifiers

Catalog Number
098-4 FDA UDI
Primary DI / UDI-DI
00851329005258 FDA UDI
FDA Product Code
PQY FDA UDI
GMDN Term
Hand-held deep-tissue electromagnetic stimulator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5290 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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hand-held deep-tissue electromagnetic stimulator

ActiPatch by Bioelectronics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held deep-tissue electromagnetic stimulator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bioelectronics Corporation

Sources (1)

  • FDA UDI bda85887-452e-423c-a3ea-f51cf3437d24 36 fields · synced Jun 1, 2026