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Otoport Pro Display Window service item

FDA UDI

Class II (US FDA UDI)

by Otodynamics

Identity

Trade Name
Otoport Pro Display Window service item FDA UDI
Generic Name
Otoacoustic emission system, battery-powered FDA UDI
Device Name
Display Window service part for Otoport Pro (for authorised dealers/repair centres only) FDA UDI
Model / Reference
OP2-WIN FDA UDI
Description
Display Window service part for Otoport Pro (for authorised dealers/repair centres only) FDA UDI

Identifiers

Primary DI / UDI-DI
05060396173622 FDA UDI
510(k) Number
K240430 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Otoport Pro Display Window service item by Otodynamics — 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
Otodynamics

Sources (1)

  • FDA UDI f20b6d4a-b425-4fb9-8e20-41a3c019a877 35 fields · synced Jun 8, 2026