ELINE S.R.L.
Italy IT-MF-000029568 Last updated 17 Sep 2026
- Devices
- 145
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
SecurEline® Carta crespata | Crepe paper Ref 20710060
SecurEline® Carta crespata | Crepe paper Ref 20710051
SecurEline® Carta crespata | Crepe paper Ref 20620050
SecurEline® Carta crespata | Crepe paper Ref 20710034
Medibase Sterilization reels Ref 20430083
SecurEline® Carta crespata | Crepe paper Ref 20710009
SecurEline® Carta crespata | Crepe paper Ref 20710012
SecurEline® Carta crespata | Crepe paper Ref 20710101
SecurEline® Carta crespata | Crepe paper Ref 20710002
SecurEline® Carta crespata | Crepe paper Ref 20710057
SecurEline® Carta crespata | Crepe paper Ref 20710061
SecurEline® Carta crespata | Crepe paper Ref 20710004
SecurEline® Carta crespata | Crepe paper Ref 20620119
SecurEline® Carta crespata | Crepe paper Ref 20710031
Showing 101-145 of 145
What ELINE S.R.L. makes
Eline S.R.L. manufactures medical sterilization materials, including rolls of sterilization paper, crepe paper, and self-adhesive sterilization pouches designed for use in healthcare settings. These products are intended to protect surgical instruments and devices during sterilization processes, ensuring barrier integrity and compliance with sterilization protocols.
The company’s products fall under Class I medical devices and are listed in the EUDAMED database, adhering to European Union regulatory requirements. Eline S.R.L. is based in Italy and operates within the scope of EU medical device regulations.
Frequently asked questions
What types of medical devices does Eline S.R.L. manufacture?
Eline S.R.L. specializes in medical sterilization materials, including sterilization rolls, crepe paper, and self-adhesive sterilization pouches. These products are designed to create protective barriers for surgical instruments and devices during sterilization, ensuring they remain uncontaminated and compliant with sterilization standards in healthcare settings.
Where is Eline S.R.L. based, and how does this affect its regulatory compliance?
Eline S.R.L. is based in Italy, which places its devices under the jurisdiction of the European Union’s medical device regulations. Since its products are listed in the EUDAMED database, they must comply with EU requirements, including classification under the Medical Device Regulation (MDR) or In Vitro Diagnostic Regulation (IVDR) where applicable.
Which regulatory registries list Eline S.R.L.’s devices, and why is this important?
Eline S.R.L.’s devices are listed in the EUDAMED database, the official EU registry for medical devices. This listing confirms that the company has reported its products to national competent authorities, fulfilling transparency requirements under EU regulations. Listing in EUDAMED ensures traceability and compliance with regulatory obligations for Class I devices.
How are Eline S.R.L.’s sterilization materials classified under EU regulations?
Eline S.R.L.’s sterilization materials, such as rolls, pouches, and crepe paper, are classified as Class I medical devices under EU regulations. This classification applies because these products pose minimal risk to patients and users, primarily serving as protective barriers during sterilization rather than actively influencing treatment outcomes.
Information
- Country
- Italy
- Address
- 7, Via dell'Artigianato, Montecchio Precalcino, Italy
- Website
- elineitalia.com
- [email protected]
- Phone
- +39 0445 334455
- PRRC contact
- Galeno Pietro Rossato
- EUDAMED SRN
- IT-MF-000029568