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Bo-ject DHN Disp Electrode, 1.5"(37mm)x0.46mm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 9013S0472

by Natus Manufacturing Limited

Identity

Trade Name
Bo-ject DHN Disp Electrode, 1.5"(37mm)x0.46mm EUDAMED
Boject FDA UDI
Generic Name
Electromyographic needle electrode, single-use FDA UDI
Device Name
Bo-Ject® DHN Disposable Hypodermic Needle Electrodes EUDAMED
Bo-ject Needle FDA UDI
Model / Reference
9013S0472 EUDAMEDFDA UDI
Description
Bo-ject Needle FDA UDI

Identifiers

Primary DI / UDI-DI
00382830042451 EUDAMEDFDA UDI
Basic UDI-DI
038283NA00007DZ EUDAMED
Unit of Use DI
00382830062633 EUDAMED
FDA Product Code
IKT FDA UDI
EMDN Code
Z12100485 ELECTROMYOGRAPHY INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Electromyographic needle electrode, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
890.1385 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

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

Bo-ject DHN Disp Electrode, 1.5"(37mm)x0.46mm by Natus Manufacturing Limited — Class IIa — 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 3911cf0f-0b76-45f4-8a9d-8aab10afdf86 61 fields · synced Jul 17, 2026
  • FDA UDI f03a59d3-d2ca-45fd-831d-28598f634d89 33 fields · synced May 30, 2026