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Natus EMG Cables

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9013C0312

by Natus Manufacturing Limited

Identity

Trade Name
Natus EMG Cables EUDAMED
Keypoint FDA UDI
Generic Name
Electromyographic needle electrode, single-use FDA UDI
Device Name
Natus EMG Cables EUDAMED
Hush™ Reusable Yoke Cable Straight 5-pin DIN to three 1.5mm male touchproof connectors plus a female 5-pin DIN, 1.5m(59"), 1/pkg FDA UDI
Model / Reference
9013C0312 EUDAMEDFDA UDI
Description
Hush™ Reusable Yoke Cable Straight 5-pin DIN to three 1.5mm male touchproof connectors plus a female 5-pin DIN, 1.5m(59"), 1/pkg FDA UDI

Identifiers

Catalog Number
9013C0312 FDA UDI
Primary DI / UDI-DI
00382830047821 EUDAMEDFDA UDI
Basic UDI-DI
0382830059046TZ EUDAMED
FDA Product Code
IKD FDA UDI
EMDN Code
N010101 ELECTROMYOGRAPHIC ELECTRODES EUDAMED
GMDN Term
Electromyographic needle electrode, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
890.1175 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Natus EMG Cables by Natus Manufacturing Limited — 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
IE-MF-000000799

Sources (2)

  • EUDAMED 4712fb34-dfc1-4e21-8531-f7973f3a06a2 61 fields · synced Jun 18, 2026
  • FDA UDI 8fc943ca-3cd9-4f92-bcd6-8366eaa650c2 34 fields · synced May 30, 2026