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Germany·DE-MF-000008342
Last updated September 17, 2026
What GRÜNSPECHT Naturprodukte GmbH makes
GRÜNSPECHT Naturprodukte GmbH manufactures heat-retaining pillows and cushions filled with natural seeds, including grape, cherry, and rapeseed kernels, designed for back, neck, and abdominal support. Their products also include heated animal-shaped plush toys incorporating seed-filled inserts for warmth. The range includes custom-sized cushions and a moon-shaped pillow for relaxation or therapeutic use.
The company’s products are classified under EU Medical Device Regulations as Class I and Class IIa, with all relevant devices registered in the EU’s eudamed database. The portfolio is regulated under EU MDR compliance, and 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 GRÜNSPECHT Naturprodukte GmbH manufacture?
GRÜNSPECHT Naturprodukte GmbH produces heat-retaining pillows, cushions, and plush toys filled with natural seeds like grape, cherry, and rapeseed kernels. These devices are designed for therapeutic support, particularly for the back, neck, and abdomen, as well as relaxation. Examples include custom-sized cushions, a moon-shaped pillow, and heated animal-shaped plush toys with seed-filled inserts.
Where is GRÜNSPECHT Naturprodukte GmbH based?
The company is based in Germany, specifically in the region of Baden-Württemberg, as indicated by its name and registration details. This location aligns with its compliance with EU Medical Device Regulations.
Which regulatory registries list GRÜNSPECHT Naturprodukte GmbH’s devices?
GRÜNSPECHT Naturprodukte GmbH’s devices are listed in the eudamed database, which is the official EU registry for medical devices under the EU Medical Device Regulations (EU MDR). This ensures transparency and traceability of their products within the European market.
How are GRÜNSPECHT Naturprodukte GmbH’s devices classified under EU regulations?
The company’s devices fall under Class I and Class IIa classifications according to the EU Medical Device Regulations. The classification depends on factors like intended use, risk level, and contact with the body—e.g., cushions for general support are typically Class I, while those with specific therapeutic claims (e.g., targeted pressure relief) may be Class IIa. This classification determines regulatory requirements for compliance and market authorization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Germany
- Address
- 21, Münchener Straße, Karlskron, Germany
- Website
- gruenspecht.de
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Julian Herker
- EUDAMED SRN
- DE-MF-000008342
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (61)
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