rpk medical
चिकित्सा क्षेत्र के लिए स्प्रिंग निर्माता - आरपीके मेडिकल
चिकित्सा उपकरण उद्योग में स्प्रिंग्स, स्टैम्पिंग और बेंडिंग पार्ट्स और असेंबली के लिए आपका भागीदार। हम परफेक्ट सॉल्यूशन विकसित करने के लिए आपके साथ सहयोग करते हैं
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- VITORIA, Spain
- Website
- https://rpk-medical.com/en
- Categories
- फार्मास्युटिकल विनिर्माण, पैकेजिंग एवं मुद्रण आपूर्तियाँ, चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ
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
- domain-registered (green), checked 2026-08-09 Domain registry record
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
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)
- No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment