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Sonicator Plus 930, 2 channel

FDA UDI

Class II (US FDA UDI)

by Mettler Electronics Corp.

Identity

Trade Name
Sonicator Plus 930, 2 channel FDA UDI
Generic Name
Physical therapy ultrasound/neuromuscular stimulation system FDA UDI
Device Name
Combination Therapy features a 1 and 3 MHz, 5 cm2 applicator FDA UDI
Model / Reference
ME 930 FDA UDI
Description
Combination Therapy features a 1 and 3 MHz, 5 cm2 applicator FDA UDI

Identifiers

Catalog Number
ME 930 FDA UDI
Primary DI / UDI-DI
00816864020227 FDA UDI
510(k) Number
K013192 FDA UDI
FDA Product Code
IMI FDA UDI
LIH FDA UDI
GZJ FDA UDI
IPF FDA UDI
GMDN Term
Physical therapy ultrasound/neuromuscular stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5300 FDA UDI
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

Yes

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

Dimensions & Sizes

Size
Weight — 8.7 Pound FDA UDI

Category: Physical therapy ultrasound/neuromuscular stimulation system

Sonicator Plus 930, 2 channel by Mettler Electronics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy ultrasound/neuromuscular stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mettler Electronics Corp.

Sources (1)

  • FDA UDI f912786c-18b6-494b-847b-1c538d3172d6 38 fields · synced Jun 8, 2026