← Back to catalogue

Reusable HushTM Shielded Digital Ring Electrode

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9013S0302

by Natus Manufacturing Limited

Identity

Trade Name
Reusable HushTM Shielded Digital Ring Electrode EUDAMED
Keypoint FDA UDI
Generic Name
Electromyographic needle electrode, single-use FDA UDI
Device Name
EMG Electrodes and Accessory Products EUDAMED
Reusable HushTM Shielded Digital Ring Electrode FDA UDI
Model / Reference
9013S0302 EUDAMEDFDA UDI
Description
Reusable HushTM Shielded Digital Ring Electrode FDA UDI

Identifiers

Catalog Number
9013S0302 FDA UDI
Primary DI / UDI-DI
00382830047913 EUDAMEDFDA UDI
Basic UDI-DI
0382830059183UC EUDAMED
510(k) Number
K934580 FDA UDI
FDA Product Code
GXY 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
882.1320 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Reusable HushTM Shielded Digital Ring Electrode by Natus Manufacturing Limited — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IE-MF-000000799

Sources (2)

  • EUDAMED 020f8abb-fe65-45ed-ac8d-6849fa6de737 61 fields · synced Jul 24, 2026
  • FDA UDI bc920ad8-5cb2-4de8-856e-187bff6e163d 35 fields · synced May 29, 2026