International Animal Rights Limited
Fabrication de médicaments inscrite au registre des sociétés néo-zélandaises
INTERNATIONAL ANIMAL RIGHTS LIMITED est inscrite au registre du New Zealand Companies Office sous NZBN 9429052515033, statut Enregistré au moment du contrôle, enregistré le 09/12/2024. Le registre enregistre la classification industrielle « Medicine mfg » (ANZSIC C184120), qui place l'entreprise dans la fabrication plutôt que dans le commerce, et répertorie vita-chemicals.com comme site Web.
- Type
- brand seeking distribution
- Location
- Auckland, New Zealand
- Founded
- 2024
- Website
- https://vita-chemicals.com
- Categories
- Fournitures médicales et de santé
- Markets
- Nouvelle-Zélande
Listed in a source registry
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-23 Mail server of the company domain
- domain-registered (green), checked 2026-08-23 Domain registry record
- registered-activity (green), checked 2026-08-24 https://www.nzbn.govt.nz/mynzbn/nzbndetails/9429052515033/
- registered-address (green), checked 2026-08-24 https://www.nzbn.govt.nz/mynzbn/nzbndetails/9429052515033/
- registry-active-global (green), checked 2026-08-21 New Zealand Companies Office (NZBN bulk data)
- debarment-clear (green), checked 2026-08-23 OpenSanctions
- sanctions-clear (green), checked 2026-08-23 OpenSanctions
- 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)
- 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)