PT Alterlab Teknologi Indonesia
연구 및 산업을 위한 실험실 장비 및 기술
PT Alterlab Teknologi Indonesia는 국제 제조업체의 실험실 장비와 기술을 유통합니다. 인도네시아의 연구원, 기업, 대학 및 산업 연구소에 제품을 공급합니다.
- 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
- 산업용품, 산업기계, 의료 및 건강 관리 용품
- Markets
- 인도네시아
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