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Software Update to v22.3

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 688-628600

by Natus Neurology Incorporated

Identity

Trade Name
Software Update to v22.3 EUDAMED
Natus FDA UDI
Generic Name
Electromyograph FDA UDI
Device Name
Nicolet EDX EUDAMED
EMG Software Update to v22.3 FDA UDI
Model / Reference
688-628600 EUDAMEDFDA UDI
Description
EMG Software Update to v22.3 FDA UDI

Identifiers

Primary DI / UDI-DI
00382830036153 EUDAMEDFDA UDI
Basic UDI-DI
038283NA00151E9 EUDAMED
FDA Product Code
GWF FDA UDI
EMDN Code
Z12100482 ELECTROMYOGRAPHY INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED
GMDN Term
Electromyograph FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
882.1870 FDA UDI
Market of Registration
Ireland 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Software Update to v22.3 by Natus Neurology Incorporated — Class IIb — 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
US-MF-000004246
Authorised Representative
Natus Manufacturing Ltd IE-AR-000000884

Sources (2)

  • EUDAMED b24eb750-0c2a-4c8d-8ace-27de59fe117e 61 fields · synced Oct 6, 2026
  • FDA UDI 09573739-453c-47e9-9930-4cc6bfe83b8a 33 fields · synced May 30, 2026