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ECochG Adapters

FDA UDI

Class II (US FDA UDI)

by Vivosonic Inc

Identity

Trade Name
ECochG Adapters FDA UDI
Generic Name
Otoacoustic emission system, battery-powered FDA UDI
Model / Reference
E-110 FDA UDI

Identifiers

Primary DI / UDI-DI
00627908020185 FDA UDI
510(k) Number
K043396 FDA UDI
FDA Product Code
EWO FDA UDI
GWJ FDA UDI
GMDN Term
Otoacoustic emission system, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1050 FDA UDI
882.1900 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

Yes

FDA UDI

Category: Evoked-potential audiometerOtoacoustic emission system, battery-powered

ECochG Adapters by Vivosonic Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Otoacoustic emission system, battery-powered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vivosonic Inc

Sources (1)

  • FDA UDI 6129ef25-6b7c-4e18-9051-f3ccf2a5a2eb 33 fields · synced Jun 1, 2026