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GN Otometrics A/S

FDA UDI

Class II (US FDA UDI)

by Natus Medical Denmark ApS

Identity

Trade Name
GN Otometrics A/S FDA UDI
Generic Name
Hearing aid tester, electrical FDA UDI
Model / Reference
Elevation plate FDA UDI

Identifiers

Primary DI / UDI-DI
05713315000126 FDA UDI
FDA Product Code
ETW FDA UDI
GMDN Term
Hearing aid tester, electrical 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hearing aid tester, electrical

GN Otometrics A/S by Natus Medical Denmark ApS — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hearing aid tester, electrical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cc626f9d-b6b0-4e29-86f8-fbaaa354c550 32 fields · synced May 30, 2026