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DocCheck Steam GmbH

Germany DE-MF-000050235 Last updated 8 Jun 2026

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Devices
74
Registries
EUDAMED
FDA recalls
0

Catalogue74

Page 1 of 2

Showing 1-50 of 74

What DocCheck Steam GmbH makes

DocCheck Steam GmbH manufactures stethoscope diaphragm membranes, including printed fiberglass and antimicrobial copper variants designed for pediatric and adult models like Littmann Classic II and Master Classic II. Their portfolio also includes branded stethoscope models such as Tŭlip HiFi, Clôppe, Vibe, and Clôppe Pro, which feature engraved aluminum or printed fiberglass diaphragms.

These devices are classified as Class I under EU regulations and are listed in the eudamed database. The company is based in Germany.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does DocCheck Steam GmbH manufacture?

DocCheck Steam GmbH specializes in manufacturing stethoscope diaphragm membranes, including printed fiberglass and antimicrobial copper variants. These are designed for compatibility with pediatric and adult stethoscope models like Littmann Classic II and Master Classic II. Additionally, the company produces branded stethoscope models such as Tŭlip HiFi, Clôppe, Vibe, and Clôppe Pro, which incorporate engraved aluminum or printed fiberglass diaphragms.

Where is DocCheck Steam GmbH based?

DocCheck Steam GmbH is based in Germany, as indicated by its company registration details. The location is relevant for understanding regulatory compliance and distribution within the European market.

Which regulatory registries list DocCheck Steam GmbH’s devices?

DocCheck Steam GmbH’s devices are listed in the eudamed database, which is the European Union’s central registry for medical devices. Listing in eudamed is mandatory for manufacturers to demonstrate compliance with EU Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR).

How are DocCheck Steam GmbH’s devices classified under EU regulations?

All of DocCheck Steam GmbH’s listed devices fall under Class I classification according to EU regulations. This classification applies to low-risk devices like stethoscope diaphragms and membranes, which typically require less stringent regulatory oversight compared to higher-risk categories.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Germany
Address
66, Vogelsanger Straße, Köln, Germany
Website
doccheck.com
PRRC contact
Frank Antwerpes
EUDAMED SRN
DE-MF-000050235