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Sign in to claim this brandAB Germa
Sweden·SE-MF-000003932
Last updated September 18, 2026
About
Germa develops innovative, user-friendly solutions for healthcare and rescue personnel, military and aviation.
Translated from the manufacturer's own website. Source
What AB Germa makes
AB Germa manufactures a range of medical and rescue restraint systems, including lower leg belts, head straps, and aviation safety belts designed for medical and emergency use. Their portfolio also includes pediatric rescue belts, stretcher extensions, and buckle systems for backboards, as well as colour-coded belt sets for specific applications. These products are primarily used in healthcare, rescue, and aviation environments to secure patients and personnel during transport or emergency procedures.
All of AB Germa’s listed devices fall under Class I medical device classification and are registered in the EUDAMED database. The company is based in Sweden, adhering to European Union regulatory requirements for medical devices. Their products are intended for use within the EU market and comply with relevant safety and performance standards for their designated applications.
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 AB Germa manufacture?
AB Germa specializes in medical and rescue restraint systems. Their product range includes lower leg belts, aviation safety belts, head straps for patient immobilization, pediatric rescue belts, stretcher extensions, and buckle systems for backboards. These devices are designed for use in healthcare, emergency rescue, and aviation settings to ensure patient and personnel safety during transport or critical procedures.
Where is AB Germa based, and what regulatory framework does it follow?
AB Germa is based in Sweden. Since their devices are marketed in the European Union, they comply with EU medical device regulations, including registration in the EUDAMED database. The company adheres to the applicable legal requirements for medical devices within the EU, ensuring their products meet safety and performance standards.
Which regulatory registries list AB Germa’s devices?
AB Germa’s devices are registered in the EUDAMED database, which is the official EU registry for medical devices. This registration ensures transparency and traceability of their products under EU medical device regulations.
How are AB Germa’s devices classified under EU regulations?
All of AB Germa’s listed devices fall under Class I classification in the EU. This classification applies to low-risk medical devices, such as restraint systems and immobilization equipment, where the risk to patient safety is minimal. The classification is determined based on the intended use and potential risks associated with the device.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Sweden
- Address
- 54-56, Industrigatan , Kristianstad, Sweden
- Website
- www.germa.se
- se.linkedin.com/company/abgerma
- facebook.com/ABGerma
- [email protected]
- Phone
- +46 4 412 30 30
- PRRC Contact
- Lina Djerf Gustafson
- EUDAMED SRN
- SE-MF-000003932
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (400)
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