NATEC Medical Ltd.
Mauritischer Hersteller, Entwurf und Herstellung von Angioplastie-Ballonkathetern für int
NATEC Medical Ltd. ist ein mauritischer Hersteller mit Sitz in Ebene, der im Jahr 2000 gegründet wurde. Branchen: Entwicklung und Herstellung von Angioplastie-Ballonkathetern für die interventionelle Kardiologie, Radiologie, Gastroenterologie und Urologie. Das Unternehmen ist Mitglied der Mauritius Chamber of Commerce and Industry (MCCI).
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ebene, Mauritius
- Founded
- 2000
- Website
- https://natec-medical.com
- Categories
- Medizin- & Gesundheitsbedarf
- Markets
- Mauritius
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 2026-08-09 Mail server of the company domain
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- domain-registered (green), checked 2026-08-09 Domain registry record
- tax-filing-active (green), checked 2026-08-21 Mauritius Revenue Authority (MRA), List of VAT Registered Persons
- registry-id-verified (green), checked 2026-08-21 List of VAT Registered Persons (MRA, Mauritius)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- fda-registered (green), checked 2026-08-09 FDA
- sanctions-clear (green), checked 2026-08-09 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)