DocCheck Steam GmbH
Germany DE-MF-000050235 Last updated 8 Jun 2026
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- Devices
- 74
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Bedruckte Fiberglas-Membransets "Drums" Ref 104495.7
Bedruckte Fiberglas-Membransets "Drums" Ref 104495.2
Bedruckte Fiberglas-Membransets "Drums" Ref 104495.3
Bedruckte Fiberglas-Membransets "Drums" Ref 105001.3
Bedruckte Fiberglas-Membransets "Drums" Ref 104495.5
Bedruckte Fiberglas-Membransets "Drums" Ref 105001.7
Bedruckte Fiberglas-Membransets "Drums" Ref 104495.6
Bedruckte Fiberglas-Membransets "Drums" Ref 105001.5
Bedruckte Fiberglas-Membransets "Drums" Ref 103097.5
Bedruckte Fiberglas-Membransets "Drums" Ref 104495.4
Bedruckte Fiberglas-Membransets "Drums" Ref 105001.6
Bedruckte Fiberglas-Membransets "Drums" Ref 105001.4
Bedruckte Fiberglas-Membransets "Drums" Ref 105001.1
Bedruckte Fiberglas-Membransets "Drums" Ref 105001.0
Bedruckte Fiberglas-Membransets "Drums" Ref 105001.2
Bedruckte Fiberglas-Membransets "Drums" Ref 104495.8
Gravierte Alu-Membransets "Drums" Ref 103395.3
Bedruckte Fiberglas-Membransets "Drums" Ref 103097.4
Gravierte Alu-Membransets "Drums" Ref 104495.1
Bedruckte Fiberglas-Membransets "Drums" Ref 104495.0
Bedruckte Fiberglas-Membransets "Drums" Ref 102972.0
Gravierte Alu-Membransets "Drums" Ref 103435.1
Clôppe Ref 101650.0
Gravierte Alu-Membransets "Drums" Ref 104361.0
Bedruckte Fiberglas-Membransets "Drums" Ref 103096.16
Bedruckte Fiberglas-Membransets "Drums" Ref 103096.11
Tŭlip HiFi Ref 102527.5
Bedruckte Fiberglas-Membransets "Drums" Ref 104360.1
Bedruckte Fiberglas-Membransets "Drums" Ref 103096.12
Gravierte Alu-Membransets "Drums" Ref 104361.2
Clôppe Ref 101649.5
Gravierte Alu-Membransets "Drums" Ref 103395.0
Bedruckte Fiberglas-Membransets "Drums" Ref 102853.7
Bedruckte Fiberglas-Membransets "Drums" Ref 103096.13
Bedruckte Fiberglas-Membransets "Drums" Ref 103096.9
Bedruckte Fiberglas-Membransets "Drums" Ref 102853.2
Clôppe Ref 101650.2
Bedruckte Fiberglas-Membransets "Drums" Ref 103096.15
Vibe Ref 102510.1
Bedruckte Fiberglas-Membransets "Drums" Ref 102853.4
Bedruckte Fiberglas-Membransets "Drums" Ref 102853.6
Clôppe Ref 101649.2
Bedruckte Fiberglas-Membransets "Drums" Ref 102853.3
Clôppe Pro Ref 102956.1
Bedruckte Fiberglas-Membransets "Drums" Ref 104360.4
Bedruckte Fiberglas-Membransets "Drums" Ref 103096.17
Gravierte Alu-Membransets "Drums" Ref 104361.1
Clôppe Ref 101649.1
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.
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.
Information
- Country
- Germany
- Address
- 66, Vogelsanger Straße, Köln, Germany
- Website
- doccheck.com
- [email protected]
- PRRC contact
- Frank Antwerpes
- EUDAMED SRN
- DE-MF-000050235