Laboratorios Andrómaco
Dermatoloji, ilaç ve kişisel bakım üreticisi.
Laboratorios Andrómaco, Arjantin'den dermatoloji ilaçları, yara bakımı, cilt bakımı ve kişisel bakım ürünleri üretmektedir. Şirket eczanelere, hastanelere ve bölgesel sağlık distribütörlerine ürün tedarik etmektedir.
- 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
- Tıbbi ve Sağlık Malzemeleri, Cilt Bakımı ve Kozmetik
- Markets
- Arjantin, Şili, 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)