Laboratorios Andrómaco
Fabricant de dermatologie, de produits pharmaceutiques et de soins personnels.
Laboratorios Andrómaco fabrique des médicaments dermatologiques, des produits de soins des plaies, des soins de la peau et des produits de soins personnels en provenance d'Argentine. L'entreprise fournit des pharmacies, des hôpitaux et des distributeurs régionaux de soins de santé.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Buenos Aires, Argentina
- Founded
- 1926
- Website
- andromaco.com
- Categories
- Fournitures médicales et de santé, Soins et cosmétiques
- Markets
- Argentine, Chili, Uruguay, Paraguay
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 2026-08-04 Mail server of the company domain
- domain-registered (green), checked 2026-08-04 Domain registry record
- sanctions-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- GMP Cosmetics (ISO 22716) IAF CertSearch
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)