Sanofi-Aventis New Zealand Limited
Medicine mfg im neuseeländischen Firmenregister eingetragen
SANOFI-AVENTIS NEW ZEALAND LIMITED ist im Handelsregister des New Zealand Companies Office unter NZBN 9429000014304 eingetragen, Status „Registriert“ zum Zeitpunkt der Prüfung, registriert am 27.01.1981. Im Register ist die Branchenklassifikation „Medicine mfg“ (ANZSIC C184120) eingetragen, die das Unternehmen eher der Fertigung als dem Handel zuordnet, und listet sanofi.com.au als Website auf.
- Type
- brand seeking distribution
- Location
- Auckland, New Zealand
- Founded
- 1981
- Website
- https://sanofi.com.au
- Categories
- Medizin- & Gesundheitsbedarf
- Markets
- Neuseeland
Listed in a source registry
Verified facts
- registered-activity (green), checked 2026-08-24 https://www.nzbn.govt.nz/mynzbn/nzbndetails/9429000014304/
- registered-address (green), checked 2026-08-24 https://www.nzbn.govt.nz/mynzbn/nzbndetails/9429000014304/
- registry-active-global (green), checked 2026-08-21 New Zealand Companies Office (NZBN bulk data)
- registered-since (green), checked 2026-08-21 New Zealand Companies Office (NZBN bulk data)
- directors-on-file (green), checked 2026-08-21 New Zealand Companies Office (NZBN bulk data)
- registry-id-verified (green), checked 2026-08-21 Companies Register (NZBN bulk data)
- lei-lapsed (amber), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-activity (green), checked 2026-08-21 New Zealand Companies Office (NZBN bulk data)
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)