Molnlycke Health Care
Apósitos para el cuidado de heridas, campos quirúrgicos, batas y guantes.
Molnlycke Health Care fabrica apósitos para el cuidado de heridas, campos quirúrgicos, batas y guantes en sus operaciones de Gotemburgo. La empresa abastece a compradores de hospitales, distribuidores clínicos, sistemas de salud o clientes de exportación en sus mercados primarios listados.
- Type
- brand seeking distribution
- Location
- Gothenburg, Sweden
- Founded
- 1849
- Website
- molnlycke.com
- Categories
- Suministros médicos y sanitarios, Suministros industriales
- Markets
- Suecia, Alemania, Estados Unidos, Reino Unido
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 Aquí la adjudicación lleva además una comprobación ajena: en la UE y el EEE el comprador público debe excluir a los licitadores condenados por fraude, corrupción o blanqueo, y a aquellos con deudas tributarias o de cotizaciones establecidas por resolución firme. 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)