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Certifications & Documentation

Clear records for confident procurement.

Company registration references and product-specific documents help your team review the proposed supply and implementation scope.

Company registrations

Registration details, in one place.

GST Certificate

33CBNPS4871D1ZE

Company tax registration reference.

Request document

Import / Export Certificate

CBNPS4871D

Importer Exporter Code (IEC).

Request document

Drug Licence Certificate

TN/CPU/20B/00715

Drug licence reference supplied by Medisky.

Request document

MD-42 Registration

TN/CPU/MD42/00008

Medical device registration reference.

Request document
Product & quality documentation

Match each document to the equipment.

The following are document categories that may be relevant to your project. Applicability and availability are reviewed for the selected manufacturer, model and supply scope.

CE

CE marking and relevant conformity documentation for the specific product, where applicable.

Review by product / scope

USFDA

Applicable US FDA clearance, approval or other device-specific records. Registration and listing alone do not establish approval.

Review by product / scope

EU

Relevant European Union product conformity documents, where applicable to the selected equipment.

Review by product / scope

BIS

Applicable Bureau of Indian Standards licence or product certification details, where required.

Review by product / scope

CDSCO

Applicable Central Drugs Standard Control Organisation licences or regulatory documents for the product and supply route.

Review by product / scope

ISO Certificate

Relevant organisation or manufacturer certificate, including the standard, certified scope, issuing body and validity.

Review by product / scope

These categories are not a claim that every Medisky product—or Medisky itself—holds every listed certification. Company registrations and product conformity documents serve different purposes.

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