Medbone-Medical Devices Lda
Von der brasilianischen Gesundheitsbehörde (ANVISA) zertifiziertes Werk
ANVISA, die brasilianische Gesundheitsbehörde, verfügt für dieses Werk über ein gültiges Good Manufacturing Practice-Zertifikat, das medizinische Geräte abdeckt und bis zum 27.11.2027 gültig ist. Das Zertifikat wird nach einer Inspektion des Werks selbst ausgestellt, weshalb eine ausländische Aufsichtsbehörde diesen Standort nennt: Hier hergestellte Waren dürfen auf den brasilianischen Markt gelangen. Prozessnummer 25351043178201912.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Portugal
- Categories
- Medizin- & Gesundheitsbedarf
- Markets
- Portugal, Brasilien
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
- 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
- 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
- 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)