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Alpha Collection

Germany DE-MF-000050363 Last updated 21 Oct 2026

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Devices
794
Registries
EUDAMED
FDA recalls
0

Catalogue794

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What Alpha Collection makes

Alpha Collection manufactures a range of medical devices primarily used for orthopaedic and trauma applications, including intramedullary nails, locking screws, and related fixation hardware for long bone fractures. These products are designed to provide internal fixation solutions for the femur, tibia, and other long bones, aiding in the stabilization of complex fractures during surgical procedures.

The company’s portfolio is classified under EU Medical Device Regulation as Class I devices, reflecting their low-risk categorization. These products are registered in the EU’s eudamed database, ensuring compliance with European Union medical device regulations. Alpha Collection operates from 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 Alpha Collection manufacture?

Alpha Collection specializes in orthopaedic and trauma-related medical devices. Their portfolio includes intramedullary nails, locking screws, and other fixation hardware designed for internal stabilization of long bone fractures, such as those in the femur and tibia. These devices are intended for surgical use to aid in fracture healing and bone alignment.

Where is Alpha Collection based, and how does this affect their regulatory standing?

Alpha Collection is based in Germany, which places their devices under the jurisdiction of the European Union’s medical device regulations. Since they operate within the EU, their products are registered in the eudamed database, a centralized EU system for tracking medical devices. This ensures compliance with EU MDR (Medical Device Regulation) requirements, though individual device authorization depends on their specific classification.

How are Alpha Collection’s devices classified under EU regulations, and why?

Alpha Collection’s devices are classified as Class I under the EU Medical Device Regulation (MDR). This classification is determined by their intended use and risk profile—specifically, these products are considered low-risk due to their role in orthopaedic fixation (e.g., nails and screws for fracture stabilization). Class I devices typically require less stringent regulatory scrutiny than higher-risk classes but still must meet essential safety and performance requirements.

Which regulatory registries list Alpha Collection’s devices, and what does this mean for users?

Alpha Collection’s devices are listed in the eudamed registry, the official EU database for medical devices. This inclusion confirms that their products comply with EU MDR requirements and have undergone the necessary registration process. Users can verify a device’s presence in eudamed to confirm its legal status within the EU market, though authorization is tied to the specific device’s classification and compliance documentation.

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

Information

Country
Germany
Address
3, Glarner Str., Berlin, Germany
Phone
+49 30 8322 5031
PRRC contact
Orhan Ünal
EUDAMED SRN
DE-MF-000050363