Sterile Bio-Adhesive (SURGBOND) - FDA Registration d613e7a8dc9e77bc67e5d673e739be47
Access comprehensive regulatory information for Sterile Bio-Adhesive (SURGBOND) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d613e7a8dc9e77bc67e5d673e739be47 and manufactured by Nectar Laboratories Private Limited. The device was registered on August 17, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
d613e7a8dc9e77bc67e5d673e739be47
Sterile Bio-Adhesive (SURGBOND)
FDA ID: d613e7a8dc9e77bc67e5d673e739be47
Device Classification
Brand Name
SURGBOND
Registration Information
Analysis ID
d613e7a8dc9e77bc67e5d673e739be47
Registration Date
August 17, 2022
Manufacturer
Authorized Representative

