OLTB025

Organization name

Dent-A-Pharm Produktionsgesellschaft mbH

SRN

DE-MF-000012922

Manufacturer status

Active

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

• CW082

  EUDAMED did not publish a description for this code.
• CW162

  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.
• CW305

  EUDAMED did not publish a description for this code.
• CW449

  EUDAMED did not publish a description for this code.
• CW456

  EUDAMED did not publish a description for this code.
• CW085

  EUDAMED did not publish a description for this code.
• CW416

  EUDAMED did not publish a description for this code.
• CW397

  EUDAMED did not publish a description for this code.
• CW304

  EUDAMED did not publish a description for this code.
• CW090

  EUDAMED did not publish a description for this code.
• CW164

  EUDAMED did not publish a description for this code.
• CW401

  EUDAMED did not publish a description for this code.
• CW299

  EUDAMED did not publish a description for this code.
• CW148

  EUDAMED did not publish a description for this code.

Primary placement in Germany; available across 32 countries total.

Trade name

not provided

UDI-DI code

+D932OLTB0251W

Basic UDI-DI

B-+D932OLTB0251W

Reference / catalog number

OLTB025

Issuing entity

HIBCC

Risk category

Class IIa

Applicable legislation

MDD [Directive 93/42/EEC 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

+D932OLTB0251W

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

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

• Q01010104DENTAL BONDING AGENTS