Organization name

YDM CORPORATION

SRN

JP-MF-000011653

Manufacturer status

Active

Primary placement in Spain; available across 12 countries total.

Trade name

GP Remover Double Edge Dome 0.3L(Yellow)

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

04963931271283

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

4963931YDM00006WQ

Reference / catalog number

27128

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

http://www.ydm.co.jp/en-new/

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• L159003DENTAL AND PERIODONTAL PROBES AND EXPLORERS, REUSABLE

• Class I medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.