PT Anugerah Pharmindo Lestari
फार्मास्युटिकल और स्वास्थ्य देखभाल उत्पाद वितरण नेटवर्क
एक फार्मास्युटिकल वितरण कंपनी जो फार्मेसियों, अस्पतालों और स्वास्थ्य सुविधाओं को दवाओं, चिकित्सा उपकरणों और स्वास्थ्य देखभाल उत्पादों की आपूर्ति करती है।
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Indonesia
- Website
- aplcare.com
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ, पूरक और कल्याण
- Markets
- इंडोनेशिया
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
- domain-registered (green), checked 2026-08-04 Domain registry record
- product-authorised-for-sale (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of products authorised for sale in Indonesia (Cek Produk)
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- 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
- 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
- facility-registered (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of manufacturing facilities behind product registrations (Sarana)
- registered-trade-role (green), checked 2026-08-19 Kemenkes e-Sertifikasi Alkes (Ministry of Health of Indonesia), medical-device certification lists
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- 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)