Ceramed - Ceramicos Para Aplicações Médicas S.A
Tanaman disertifikasi oleh regulator kesehatan Brasil (ANVISA)
ANVISA, regulator kesehatan Brasil, memegang sertifikat Praktik Manufaktur yang Baik untuk pabrik ini, yang mencakup peralatan medis, yang berlaku hingga 07-10-2026. Sertifikat tersebut dikeluarkan setelah inspeksi terhadap pabrik itu sendiri, itulah sebabnya regulator asing menamai situs ini: barang yang dibuat di sini diperbolehkan di pasar Brasil. Sertifikat mencatat alamat situs sebagai RUA JOSÉ GOMES FERREIRA, N.º 1, ARMAZÉM D, SÃO JULIÃO DO TOJAL, LOURES 2660-360. Nomor proses 25351426377201954.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Lisboa, Portugal
- Categories
- Perlengkapan Medis & Kesehatan
- 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)