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Trumpet

FDA UDI

Class II (US FDA UDI)

by Inventis Srl

Identity

Trade Name
TRUMPET FDA UDI
Generic Name
Ear canal insertion gain measurement instrument FDA UDI
Device Name
The kit includes loudspeaker, coupler, microphone, and the adapters in order to perform RECD measurements on different types of hearing aids. FDA UDI
Model / Reference
KIT FOR RECD MEASUREMENTS WITH LOUDSPEAKER FUNCTION FDA UDI
Description
The kit includes loudspeaker, coupler, microphone, and the adapters in order to perform RECD measurements on different types of hearing aids. FDA UDI

Identifiers

Catalog Number
11167 FDA UDI
Primary DI / UDI-DI
08054187380624 FDA UDI
FDA Product Code
ETW FDA UDI
GMDN Term
Ear canal insertion gain measurement instrument FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3310 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ear canal insertion gain measurement instrument

Trumpet by Inventis Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ear canal insertion gain measurement instrument.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inventis Srl

Sources (1)

  • FDA UDI 1c07814a-0ea0-4241-991f-719e5a066100 35 fields · synced May 30, 2026