Organization name

Weldon Instruments

SRN

PK-MF-000010180

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• Caution

  Clean, Disinfect & Sterilize Prior to Each Use

Primary placement in Germany; available across 32 countries total.

Trade name

Weldon Instruments

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.

05056863316524

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.

50568633reusableBT

Reference / catalog number

WD-001-001R

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

Reusable, Extracting Forceps

Additional information URL

https://www.weldoninstrument.com/

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.

• L159017DENTAL RESTORATION CARVERS, REUSABLE

• Class I medical devices in EUDAMED

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