Organization name

Dent-A-Pharm Produktionsgesellschaft mbH

SRN

DE-MF-000012922

Manufacturer status

Active

+D932WP51911D

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

11 warnings recorded — scroll inside the panel to see all entries.

• CW083

  EUDAMED did not publish a description for this code.
• CW106

  EUDAMED did not publish a description for this code.
• CW159

  EUDAMED did not publish a description for this code.
• CW165

  EUDAMED did not publish a description for this code.
• CW166

  EUDAMED did not publish a description for this code.
• CW167

  EUDAMED did not publish a description for this code.
• CW422

  EUDAMED did not publish a description for this code.
• CW354

  EUDAMED did not publish a description for this code.
• CW284

  EUDAMED did not publish a description for this code.
• CW212

  EUDAMED did not publish a description for this code.
• CW272

  EUDAMED did not publish a description for this code.

Primary placement in Germany; available across 32 countries total.

Trade name

WP PerfectPrint -Tray-

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.

+D932WP51911D

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.

++D932ResinTrayNS

Reference / catalog number

WP5191

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.

HIBCC

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

No additional information URL provided by the manufacturer.

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.

• Q010503IMPRESSION MATERIAL TRAYS, SINGLE-USE

• Class I medical devices in EUDAMED

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