Submit documents

Local agent name & Address

E-mail

Phone number (Personal)

Name of the product

Legal Manufacturer's name & address

Manufacturing site name & address

Indication/use of the device

FSC (Free sale certificate) Country of Origin

FSC - EU country/USA/Japan/Germany/Australia/UK

EC Certificate/EU MDR

ISO Certificate

Letter of Authorization

**For EU MDR Class IIb and III medical device, please, upload FSC/CFS issued from USA/any EU country/Australia/UK/Germany.

PHARMA DRA