PT Alterlab Teknologi Indonesia
معدات وتكنولوجيا المختبرات للبحث والصناعة
تقوم شركة PT Alterlab Teknologi Indonesia بتوزيع معدات وتقنيات المختبرات من الشركات المصنعة العالمية. تقوم بتزويد الباحثين والشركات والجامعات والمختبرات الصناعية في إندونيسيا.
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Depok, Indonesia
- Founded
- 2011
- Website
- alterlab.co.id
- Categories
- اللوازم الصناعية, الآلات الصناعية, اللوازم الطبية والرعاية الصحية
- Markets
- إندونيسيا
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
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- 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
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- 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
- 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)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission