BIOCERAMED - Ceramicos para Aplicacoes Medicas, S.A.
Het toekomstige leven innoveren met Bioceramed: geavanceerde orthobiologie voor botregeneratie en gezondheidszorg
Bioceramed innoveert het toekomstige leven door middel van geavanceerde orthobiologische geneesmiddelen, waaronder PRP/PRF-therapieën en viscosupplementatie, om de botregeneratie en genezing te verbeteren. Onze producten verbeteren de patiëntresultaten op het gebied van orthopedie, wervelkolomzorg en tandheelkundige behandelingen.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Barco - Guimaraes, Portugal
- Website
- https://bioceramed.com
- Categories
- Medische en gezondheidszorgbenodigdheden
- Markets
- Portugal
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-22 Mail server of the company domain
- domain-registered (green), checked 2026-08-22 Domain registry record
- sanctions-clear (green), checked 2026-08-22 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-22 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registered-manufacturer (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
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)