BIOCERAMED - Ceramicos para Aplicacoes Medicas, S.A.
バイオセラミックで未来の生活を革新: 骨の再生とヘルスケアのための高度なオルソバイオロジクス
バイオセラメッドは、骨の再生と治癒を促進するために、PRP/PRF 療法や粘性サプリメントなどの高度なオルソバイオロジクスを通じて未来の生活を革新しています。当社の製品は、整形外科、脊椎ケア、歯科治療における患者の治療成績を向上させます。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Barco - Guimaraes, Portugal
- Website
- https://bioceramed.com
- Categories
- 医療およびヘルスケア用品
- Markets
- ポルトガル
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)