Ceramed - Ceramicos Para Aplicações Médicas S.A
Planta certificada pela agência reguladora sanitária brasileira (ANVISA)
A ANVISA, órgão regulador sanitário brasileiro, possui um certificado de Boas Práticas de Fabricação válido para esta planta, abrangendo dispositivos médicos, válido até 07/10/2026. O certificado é emitido após vistoria na própria fábrica, por isso um regulador estrangeiro dá nome a este site: produtos fabricados aqui são permitidos no mercado brasileiro. O certificado regista o endereço do site como RUA JOSÉ GOMES FERREIRA, N.º 1, ARMAZÉM D, SÃO JULIÃO DO TOJAL, LOURES 2660-360. Número do processo 25351426377201954.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Lisboa, Portugal
- Categories
- Suprimentos médicos e de saúde
- Markets
- Portugal, Brasil
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
- sanctions-clear (green), checked 2026-08-24 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-24 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- manufacturing-practice-certified (green), checked 2026-08-21 ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
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)