← Back to catalogue

Megapulse III/OmniSWD

FDA UDI

Class II (US FDA UDI)

by Accelerated Care Plus Corp.

Identity

Trade Name
Megapulse III/OmniSWD FDA UDI
Generic Name
Short-wave diathermy treatment system generator FDA UDI
Device Name
Shortwave Diathermy for the use of applying therapeutic deep heat FDA UDI
Model / Reference
1903030 FDA UDI
Description
Shortwave Diathermy for the use of applying therapeutic deep heat FDA UDI

Identifiers

Primary DI / UDI-DI
00858703006085 FDA UDI
510(k) Number
K153456 FDA UDI
FDA Product Code
IMJ FDA UDI
GMDN Term
Short-wave diathermy treatment system generator 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Short-wave diathermy treatment system generator

Megapulse III/OmniSWD by Accelerated Care Plus Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Short-wave diathermy treatment system generator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Accelerated Care Plus Corp.

Sources (1)

  • FDA UDI 20975e55-984d-484c-afda-2f3dbde035ec 36 fields · synced Jun 8, 2026