Alan Electronic Systems Private Limited
Fabrikant van medische elektronische apparatuur sinds 1997
ALAN Electronic Systems Private Limited is een Indiase fabrikant van geavanceerde medische elektronische apparatuur, opgericht in 1997. Met meer dan 25 jaar expertise in elektronica en meer dan twintig jaar toegewijd aan de industrie voor medische apparatuur, zijn wij gespecialiseerd in het ontwerpen, ontwikkelen en produceren van innovatieve chirurgische apparatuur voor zorginstellingen over de hele wereld. Onze medische divisie, opgericht in 2004, richt zich op het leveren van betrouwbare, hoogwaardige oplossingen die chirurgen ondersteunen en de patiëntenzorg verbeteren.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- India
- Website
- https://alanindia.net
- Categories
- Medische en gezondheidszorgbenodigdheden, Consumentenelektronica
- 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)