Why PrecisionMed
Buying ophthalmic equipment means balancing clinical outcomes, budgets, registration and uptime. We organise our whole company around making that decision easier for you.
We are not a generalist distributor with an ophthalmic line. Eye care is all we do, so every recommendation comes from someone who understands refraction, biometry, imaging and surgical workflow and the questions your ophthalmologists will ask.
From the front-of-clinic examination lane to IOLs, OCT and retinal lasers, our range covers the complete clinical workflow. One trusted partner means one quotation, one set of import documents and one point of contact for service.
We source from certified manufacturers in Asia and Europe and move every shipment through a fully documented export-import process. Batch and serial traceability runs from manufacturer to your hospital, which is what tenders and audits require.
We understand the regulatory pathways and hospital procurement processes in Indonesia, from device registration to e-catalogue and tender documentation. Equipment arrives registered, documented and ready to install.
How we work
Tell us your institution, the procedures you offer and your timeline. We reply within one business day.
We discuss clinical goals with your ophthalmologists and recommend configurations, not just models.
A clear quotation with lead times, warranty terms and the documents your procurement team needs.
Registration status confirmed, export-import documents prepared and traceability recorded.
Coordinated delivery to your hospital, installation and calibration by trained engineers.
User training at handover, then responsive support and manufacturer service coordination.
Yes. PrecisionMed distributes ophthalmic medical equipment and devices only, covering refraction and diagnostics, slit lamps, biometry, ultrasound, IOLs, OCT, retinal lasers and the accessories that complete the examination lane.
Indonesia is our primary market, served from our Singapore headquarters. We also supply Singapore and are expanding to Malaysia, Thailand and the Philippines.
Yes. We manage the regulatory pathway for the products we distribute and advise on registration status before you tender, so the equipment you buy can legally be imported and used.
Commercial invoice, packing list, certificates of origin and conformity where applicable, and batch, serial or diopter lists for traceability. Documents are prepared to meet hospital procurement and customs requirements.
Every system is delivered with installation, calibration and user training at handover. We coordinate manufacturer service support for the life of the device.
We reply to enquiries within one business day with options and lead times. Formal quotations follow once configuration is confirmed with your clinical team.
Send us your procedure list and patient volumes. We reply within one business day with a configuration, registration status and lead times.
