Alan Electronic Systems Private Limited
Produsen peralatan elektronik medis sejak tahun 1997
ALAN Electronic Systems Private Limited adalah produsen peralatan elektronik medis canggih di India, didirikan pada tahun 1997. Dengan lebih dari 25 tahun keahlian di bidang elektronik dan lebih dari dua dekade didedikasikan untuk industri perangkat medis, kami mengkhususkan diri dalam merancang, mengembangkan, dan memproduksi peralatan bedah inovatif untuk institusi kesehatan di seluruh dunia. Divisi Medis kami, yang didirikan pada tahun 2004, berfokus untuk memberikan solusi berkinerja tinggi dan andal yang mendukung ahli bedah dan meningkatkan perawatan pasien.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- India
- Website
- https://alanindia.net
- Categories
- Perlengkapan Medis & Kesehatan, Elektronik Konsumen
- Markets
- India
Listed in a source registry
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
- 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
- domain-registered (green), checked 2026-08-04 Domain registry record
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)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)