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Analogue Optocoupler

EUDAMEDFDA UDI

Class I (EU MDR)

Ref NGA100Model Optocoupler

by SOMNOmedics AG

Identity

Trade Name
Analogue Optocoupler EUDAMED
1-channel analogue optocoupler FDA UDI
Generic Name
Polysomnograph FDA UDI
Model / Reference
Optocoupler EUDAMED
NGA100 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04250413410095 EUDAMEDFDA UDI
Basic UDI-DI
42504134anaOKU9 EUDAMED
510(k) Number
K071556 FDA UDI
FDA Product Code
MNR FDA UDI
EMDN Code
Z1203020280 MULTI-PARAMETER MONITORS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Polysomnograph FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
Market of Registration
Germany 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

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

No

FDA UDI

Analogue Optocoupler by SOMNOmedics AG — 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

Manufacturer
SOMNOmedics AG
EUDAMED SRN
DE-MF-000006921

Sources (2)

  • EUDAMED b59d969f-80bc-48f4-828b-b0b6905267a1 61 fields · synced Jul 9, 2026
  • FDA UDI e4f96c46-feec-4a58-905e-e7e690f745ce 33 fields · synced May 30, 2026