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Sign in to claim this brandP.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA
Portugal·PT-MF-000010370
Last updated September 17, 2026
What P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA makes
The company manufactures reusable and single-use compression garments, including knee, thigh, and ankle supports with elastic properties, as well as knee sleeves with thermal fabric options. Their portfolio also includes ankle-foot orthoses and reusable scar-management dressings designed for medical or post-treatment support.
These devices are classified as Class I under EU regulations and are registered in the EUDAMED database. The manufacturer is based in Portugal.
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 P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA manufacture?
P.E.E.T.H. specialises in compression and support garments, primarily reusable and single-use items. Their portfolio includes knee, thigh, and ankle elastic supports, such as knee sleeves with thermal fabric options, as well as ankle-foot orthoses and reusable scar-management dressings. These devices are designed for medical or post-treatment applications, focusing on compression therapy and physical support.
Where is P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA based?
The company is based in Portugal, as indicated by its country designation (PT). This location is relevant for regulatory compliance and distribution within the European market.
Which regulatory registries list devices manufactured by P.E.E.T.H.?
Devices produced by P.E.E.T.H. are registered in the EUDAMED database, which is the European Union’s medical device registry. This platform is used to track and monitor medical devices authorised under EU regulations, ensuring transparency and traceability.
How are the devices from P.E.E.T.H. classified under EU regulations?
All devices manufactured by P.E.E.T.H. fall under Class I classification in the EU regulatory framework. This classification applies to low-risk medical devices, such as compression garments and orthoses, which typically pose minimal risk to patients when used as intended. Classification determines the regulatory pathway for authorisation.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Portugal
- Address
- 340, Estrada Luiz Bernardo de Almeida, Vale de Cambra, Portugal
- Website
- www.peeth.pt
- —
- facebook.com/ortopediapeeth
- [email protected]
- Phone
- +351 256 422 282
- PRRC Contact
- Luís Brandão
- EUDAMED SRN
- PT-MF-000010370
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (201)
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