Laboratorios Andrómaco
Nhà sản xuất da liễu, dược phẩm và chăm sóc cá nhân.
Phòng thí nghiệm Andrómaco sản xuất thuốc da liễu, chăm sóc vết thương, chăm sóc da và các sản phẩm chăm sóc cá nhân từ Argentina. Công ty cung cấp cho các hiệu thuốc, bệnh viện và nhà phân phối dịch vụ chăm sóc sức khỏe trong khu vực.
- 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
- Vật tư y tế và chăm sóc sức khỏe, Chăm sóc da và mỹ phẩm
- Markets
- Argentina, Chile, 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)