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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

11701272 — Class I MDR by Baumann Dental GmbH

MD Atlas
Baumann Dental GmbH

EUDAMED last updated this device on May 11, 2026

11701272

++EBD170100XD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Baumann Dental GmbH
UDI-DI code: +EBD1117012721
Reference / catalog number: 11701272

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Manufacturer information

Organization name: Baumann Dental GmbH
SRN: DE-MF-000010848
Manufacturer status: Active

Critical warnings

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

CW010
Gebrauchsanweisung und Desinfektionshinweise vor Anwendung beachten.
CW011
Produkt nur durch zahnmedizinisch geschultes Fachpersonal anwenden. Produkt nicht verwenden, wenn Defekte oder Beschädigungen festgestellt werden. Alle Komponenten vor Anwendung am Patienten desinfizieren. Keine alkoholbasierten Desinfektionsmittel verwenden. Produkt ist unsteril und nur zur einmaligen Verwendung bestimmt. Unsachgemäße Anwendung kann zum Verschlucken von Kleinteilen führen. Nicht anwenden bei starkem Würgereiz, PMMA-Allergie oder fehlender Kooperationsfähigkeit des Patienten.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	May 1, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: +EBD1117012721
Basic UDI-DI: ++EBD170100XD
Reference / catalog number: 11701272
Issuing entity: HIBCC

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Dental Produkt zur Bestimmung der zentralen Kieferrelation mittels Stützstiftregistrierung für prothetische Behandlungen. Zur Herstellung von 50 Stützstiftregistraten
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010299PROSTHETIC DENTISTRY DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

16100867++EBD171200XROn the market 11701270++EBD170100XDOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.