Molnlycke Health Care
Medicazioni per la cura delle ferite, teli chirurgici, camici e guanti.
Molnlycke Health Care produce medicazioni per ferite, teli chirurgici, camici e guanti dalle sue sedi di Göteborg. L'azienda fornisce acquirenti ospedalieri, distributori clinici, sistemi sanitari o clienti esportatori nei mercati primari elencati.
- Type
- brand seeking distribution
- Location
- Gothenburg, Sweden
- Founded
- 1849
- Website
- molnlycke.com
- Categories
- Forniture medicali e sanitarie, Forniture industriali
- Markets
- Svezia, Germania, Stati Uniti, Regno Unito
Verified facts
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- domain-registered (green), checked 2026-08-09 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- fda-registered (green), checked 2026-08-09 FDA
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- public-contract-awarded (green), checked 2026-08-03 TED, EU public procurement bulletin Qui l'aggiudicazione porta con sé anche un controllo altrui: nell'UE e nello SEE la stazione appaltante deve escludere gli operatori condannati per frode, corruzione o riciclaggio e quelli con debiti fiscali o contributivi accertati con decisione definitiva. Directive 2014/24/EU, Article 57 (exclusion grounds)
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- FDA Registered FDA Establishment Registration
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)