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Expertise
An experienced team with in-depth knowledge of import regulations, HS classification and clearance procedures.
Surgical products · Medical devices
Your trusted partner in medical device imports
Customs clearance for surgical products, medical devices, diagnostic kits and healthcare equipment, with DRAP Medical Devices compliance, import NOC processing and dependable release.
What this desk clears
What we handle
Every consignment type this desk files, examined and released under the correct regulatory workflow.
Clearance of surgical instruments, consumables, sutures and operating-theatre supplies.
Clearance of registered medical devices across risk classes A to D.
Clearance of in-vitro diagnostic kits, reagents and laboratory devices.
Clearance of imaging, monitoring and other electro-medical equipment.
We verify DRAP registration / Establishment Licence and process the import NOC on PSW.
Compliance with the Medical Devices Rules, 2017, matched to the device's risk class and Pakistan Customs assessment.
Medical devices and surgical products are regulated by DRAP under the Medical Devices Rules, 2017, overseen by its Medical Devices & Medical Cosmetics Division. Depending on the device and its risk class, clearance can require a valid registration, an Establishment Licence held by the local importer and an import NOC. We check exactly what your product needs and prepare the submission accordingly.
From single-use surgical consumables to Class C and D electro-medical equipment, we classify correctly, reconcile the documentation and process the import authorisation on PSW, so devices are cleared compliantly rather than held for a registration question.
Many importers bring in a mix, instruments, consumables, diagnostic kits and equipment, on the same invoice. We clear the whole consignment together, matching each line to its correct treatment, and coordinate the import NOC with the customs entry so approval and release stay in step.
Where a foreign manufacturer supplies through a local authorised representative, we work with that structure and keep the paper trail clean, shipment after shipment.
Devices and surgical products are cleared under DRAP's Medical Devices regime with Pakistan Customs.
Our process
We review invoice, packing list, B/L and DRAP registration / licence details.
We confirm registration status and prepare the import NOC request on PSW.
We follow up DRAP's Medical Devices review through to authorisation.
We file the GD on WeBOC/PSW against the device registration and NOC, then manage assessment and examination.
Devices are released and delivered safely to your facility.
Why choose us
An experienced team with in-depth knowledge of import regulations, HS classification and clearance procedures.
We ensure 100% compliance with Pakistan Customs and every relevant regulatory authority, DRAP, DPP, PTA and more.
We value your time, an efficient WeBOC/PSW process that keeps clearance and delivery on schedule.
From documentation and OGA approvals to delivery, we handle everything with professional care.
A commitment to quality that has earned us the trust of valued importers across Pakistan.
FAQ
DRAP, through its Medical Devices & Medical Cosmetics Division and the Medical Device Board, under the Medical Devices Rules, 2017. Clearance is coordinated with Pakistan Customs on WeBOC/PSW.
Requirements depend on the device and its risk class. Many devices require a valid registration and an import NOC, and the importer typically needs an Establishment Licence. We confirm the exact pathway for your product before you ship.
Devices are classified by risk from Class A (low) to Class D (high), consistent with the international model. Classification affects the registration and documentation route, we make sure your product is treated correctly.
Yes. With registration confirmed and the NOC in hand, surgical instruments and consumables clear efficiently. We prepare the NOC in parallel with the customs filing to avoid a gap.
Foreign manufacturers generally supply through a local authorised representative / market authorisation holder. We work within that structure and keep the documentation aligned for clearance.
Customs clearance for active pharmaceutical ingredients (APIs) and excipients, the raw materials your manufacturing depends on, with DRAP documentation, correct HS classification and reliable, on-time release.
Customs clearance for finished pharmaceutical medicines in every dosage form, tablets, capsules, syrups, injectables and biologicals, with DRAP registration checks, Release Order processing and careful, timely handling.
Specialist DRAP documentation and ADC processing, we prepare, file and follow up the Release Order on the Pakistan Single Window so your therapeutic goods clear customs without avoidable delay.
Get started
Get in touch with our expert team today for a quick, compliant and competitive quote.