DOCUMENTARY TRANSPARENCY
Sources and references
A public register of the sources used to contextualise the technical and regulatory information presented on flaconeosh.it.
Document register · updated 21 September 2026
How to use this register
The website pages summarise stated device information. Each reference is limited to its identified source. Where information differs, the label, official instructions for use (IFU) and current official manufacturer documentation prevail.
Source register
Public links open the original source. Documents available on request should be assessed in their current version before professional use.
- 01
PRODUCT DOCUMENT
OSH 250 ml technical catalogue · Rev. 01 · 09/2026
A product technical document published by the website. It is the reference for the stated configuration, OSH-200 identification and documentary-level information presented here.
Open the technical catalogue PDF ↗ - 02
REGULATORY FRAMEWORK
Regulation (EU) 2017/745 on medical devices
The official EUR-Lex text cited for the regulatory context and for importer and distributor roles under Articles 13 and 14. It does not replace assessments applicable to the individual device.
Read the EUR-Lex text ↗ - 03
OFFICIAL DOCUMENTATION
Label, IFU and EU declaration of conformity
These are the applicable documents for intended use, warnings, instructions and device conformity information. They are available on request from Devamed.
Request official documentation ↗ - 04
ITALIAN REFERENCE
OSH 250 ml distribution and traceability
Information page identifying Devamed S.r.l. as the Italian importer and exclusive distributor for OSH 250 ml, with contact channels and documentary references.
Open distribution and traceability ↗ - 05
IDENTIFICATION AND CONTACT
Website legal notice
The page identifies the website operator, Devamed S.r.l., and states the role of importer and exclusive distributor in Italy for OSH 250 ml, together with corporate details and contact channels.
Open the legal notice ↗
Scope and limitations
The register makes online information easier to verify, but it does not certify the content of external documents, extend the intended use or constitute medical, regulatory or legal advice.
Corrections and updates
To report information that should be corrected or request current documentation, contact Devamed at info@devamed.it.