Ceramed - Ceramicos Para Aplicações Médicas S.A
ब्राज़ीलियाई स्वास्थ्य नियामक (ANVISA) द्वारा प्रमाणित पौधा
ANVISA, ब्राज़ीलियाई स्वास्थ्य नियामक, के पास इस संयंत्र के लिए वैध गुड मैन्युफैक्चरिंग प्रैक्टिस प्रमाणपत्र है, जिसमें चिकित्सा उपकरणों को शामिल किया गया है, जो 2026-10-07 तक वैध है। प्रमाणपत्र संयंत्र के निरीक्षण के बाद ही जारी किया जाता है, यही कारण है कि एक विदेशी नियामक ने इस साइट का नाम रखा है: यहां बने सामान को ब्राजील के बाजार में अनुमति दी जाती है। प्रमाणपत्र में साइट का पता RUA JOSÉ GOMES FERREIRA, N. º 1, ARMAZÉM D, SÃO JULIÃO DO TOJAL, LOURES 2660-360 दर्ज है। प्रक्रिया क्रमांक 25351426377201954।
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Lisboa, Portugal
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ
- Markets
- पुर्तगाल, ब्राज़ील
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)