PT Alterlab Teknologi Indonesia
用于研究和工业的实验室设备和技术
PT Alterlab Teknologi Indonesia 经销来自国际制造商的实验室设备和技术。它为印度尼西亚的研究人员、公司、大学和工业实验室提供服务。
- 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
- 工业用品, 工业机械, 医疗保健用品
- Markets
- 印度尼西亚
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