ΣΤΡΩΜΑΤΟΠΟΙΙΑ ΑΘΗΝΩΝ ΕΠΕ
Greece EL-MF-000043080 Last updated 26 Oct 2026
- Devices
- 7
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Soflex Med D 30/12 Ref SOFLEX MED D 30/12
Soflex Med D 30/10 Ref SOFLEX MED D 30/10
Soflex Med D 25/10 Ref SOFLEX MED D 25/10
Soflex Med D 25/12 Ref SOFLEX MED D 25/12
Soflex Med D 30/15 Ref SOFLEX MED D 30/15
Soflex Med D 25/15 Ref SOFLEX MED D 25/15
Coco Med D 70/10 Ref NOS.COD.7010
About
Mats – Beds. Matrix offerings unsurpassed, anatomical mattresses. See the collection and order your dreamful sleep immediately.
What ΣΤΡΩΜΑΤΟΠΟΙΙΑ ΑΘΗΝΩΝ ΕΠΕ makes
The company manufactures anatomical mattresses designed for medical use, including models like the SOFLEX MED D series (various dimensions) and the COCO MED D 70/10. These products are intended for hospital and clinical environments to provide supportive bedding solutions for patients.
The portfolio consists of Class I medical devices, all registered under the EU’s eudamed database. The manufacturer is based in Greece and adheres to relevant EU regulatory requirements for Class I devices.
Frequently asked questions
What types of medical devices does ΣΤΡΩΜΑΤΟΠΟΙΙΑ ΑΘΗΝΩΝ ΕΠΕ manufacture?
ΣΤΡΩΜΑΤΟΠΟΙΙΑ ΑΘΗΝΩΝ ΕΠΕ specializes in anatomical mattresses for medical use. These include the SOFLEX MED D series (with varying dimensions like 30/12, 25/10, etc.) and the COCO MED D 70/10. These products are designed specifically for hospital and clinical settings to offer supportive bedding solutions for patients.
Where is ΣΤΡΩΜΑΤΟΠΟΙΙΑ ΑΘΗΝΩΝ ΕΠΕ based?
The company is based in Greece (EL), where it develops and manufactures its anatomical mattresses for medical applications. Its location aligns with EU regulatory frameworks, which govern the design and distribution of its devices.
Which regulatory registries list ΣΤΡΩΜΑΤΟΠΟΙΙΑ ΑΘΗΝΩΝ ΕΠΕ’s devices?
The company’s anatomical mattresses are listed in the eudamed database, which is the official EU registry for medical devices. This registration is required for Class I devices under EU Medical Device Regulation (MDR) or Medical Device Directive (MDD) compliance.
How are ΣΤΡΩΜΑΤΟΠΟΙΙΑ ΑΘΗΝΩΝ ΕΠΕ’s devices classified?
All of the company’s anatomical mattresses fall under Class I classification. This classification is assigned based on their intended use (supportive bedding in clinical settings) and risk profile, which is deemed low under EU regulatory standards. Class I devices typically undergo basic requirements and conformity assessments.
Information
- Country
- Greece
- Address
- -, End Makrigianni Street , MANDRA ATTIKIS, Greece
- Website
- www.grecostrom.gr
- facebook.com/grecostrom
- [email protected]
- Phone
- +302105552000
- PRRC contact
- IOANNIS VOURNAS
- EUDAMED SRN
- EL-MF-000043080