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Patient Responder

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 8-31-200

by Natus Medical Denmark ApS

Identity

Trade Name
Natus FDA UDI
Generic Name
Tone audiometer FDA UDI
Device Name
Patient Responder EUDAMED
Patient Responder (Black) FDA UDI
Model / Reference
8-31-200 EUDAMEDFDA UDI
Description
Patient Responder (Black) FDA UDI

Identifiers

Catalog Number
8-31-200 FDA UDI
Primary DI / UDI-DI
05713315008610 EUDAMEDFDA UDI
Basic UDI-DI
5713315NA000285E EUDAMED
FDA Product Code
EWO FDA UDI
EMDN Code
Z121401 AUDIOMETERS EUDAMED
GMDN Term
Tone audiometer FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
874.1050 FDA UDI
Market of Registration
Denmark EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Patient Responder by Natus Medical Denmark ApS — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
DK-MF-000001617

Sources (2)

  • EUDAMED 943f8c80-fbdf-41ed-bb34-8e3f127967f1 61 fields · synced Jul 24, 2026
  • FDA UDI 8d14d26b-82f5-419c-9d78-8ee741984622 34 fields · synced May 30, 2026