Sanofi-Aventis New Zealand Limited
Medicine mfg on the New Zealand companies register
SANOFI-AVENTIS NEW ZEALAND LIMITED is on the New Zealand Companies Office register under NZBN 9429000014304, status Registered at the time of the check, registered on 27/01/1981. The register records the industry classification "Medicine mfg" (ANZSIC C184120), which places the company in manufacturing rather than trade, and lists sanofi.com.au as its website.
- Type
- brand seeking distribution
- Location
- Auckland, New Zealand
- Founded
- 1981
- Website
- https://sanofi.com.au
- Categories
- اللوازم الطبية والرعاية الصحية
- Markets
- نيوزيلندا
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)