Sanofi-Aventis New Zealand Limited
Mfg di medicinali nel registro delle imprese neozelandesi
SANOFI-AVENTIS NEW ZEALAND LIMITED è iscritta nel registro delle società neozelandesi con NZBN 9429000014304, stato Registrata al momento dell'assegno, registrata il 27/01/1981. Il registro registra la classificazione industriale "Medicine mfg" (ANZSIC C184120), che colloca l'azienda nel settore manifatturiero piuttosto che in quello commerciale, ed elenca sanofi.com.au come suo sito web.
- Type
- brand seeking distribution
- Location
- Auckland, New Zealand
- Founded
- 1981
- Website
- https://sanofi.com.au
- Categories
- Forniture medicali e sanitarie
- Markets
- Nuova Zelanda
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)