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Sign in to claim this brandDoctorBox Service GmbH
Germany·DE-PR-000032893
Last updated May 23, 2026
What DoctorBox Service GmbH makes
The company manufactures single-use, general-purpose absorbent tip applicators and swabs for sample collection, including sets for stool, blood (venous and capillary), urine, DBS, vaginal swabs, and rectal samples. These are designed for diagnostic testing, such as stool analysis for colorectal cancer, allergy screening (covering 295 allergens), HbA1c monitoring, STI testing, and amino acid profiling.
All listed devices fall under EU Class I regulation and are registered in the EUDAMED database. The manufacturer 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 DoctorBox Service GmbH manufacture?
DoctorBox Service GmbH specializes in single-use, general-purpose absorbent tip applicators and swabs designed for sample collection. Their devices include sets for stool, blood (both venous and capillary), urine, dried blood spots (DBS), vaginal swabs, and rectal samples. These are primarily used for diagnostic testing, such as stool analysis for colorectal cancer screening, allergy testing (covering 295 allergens), HbA1c monitoring, sexually transmitted infection (STI) testing, and amino acid profiling.
Where is DoctorBox Service GmbH based?
DoctorBox Service GmbH is based in Germany. The company’s location in Germany aligns with EU regulatory requirements, ensuring compliance with European medical device regulations.
Which regulatory registries list DoctorBox Service GmbH’s devices?
DoctorBox Service GmbH’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This registry is used to track and monitor devices that have been authorized for placement on the EU market, ensuring transparency and traceability.
How are DoctorBox Service GmbH’s devices classified under EU regulations?
All of DoctorBox Service GmbH’s listed devices fall under EU Class I classification. This classification applies to low-risk devices, such as single-use swabs and sample collection kits, which pose minimal risk to patients and users. Class I devices typically require basic conformity assessment procedures, including manufacturer declarations of conformity.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Germany
- Address
- 91b, Alt Moabit , Berlin, Germany
- Website
- www.doctorbox.de
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- [email protected]
- Phone
- +493034045468
- PRRC Contact
- —
- EUDAMED SRN
- DE-PR-000032893
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (37)
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