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VACUETTE Serum Fluoride Tube

Bangladesh Medical Device Registration · GreinerBio-OneGmbH · Austria · B · Registered September 26, 2022

Device classification
Risk Class
B
Product Name
VACUETTE Serum Fluoride Tube
Registration information
Registration ID
665-8435-2022
Registration Date
September 26, 2022
Analysis ID
9bf1d56bb7e6839d240a4f1fa3000977
Manufacturer
Country
Austria
Authorized representative
About this record

Access comprehensive regulatory information for VACUETTE Serum Fluoride Tube in the Bangladesh medical device market through Pure Global AI's free database. This B medical device is manufactured by GreinerBio-OneGmbH in Austria. The device was registered on September 26, 2022.

This page provides complete registration details including registration ID (665-8435-2022), manufacturer information and country of origin (Austria), authorized representative (Neotec Medical Services Ltd., 235/1, Ibrahimpur, Dhaka Cantonment, Dhaka), risk classification, and regulatory compliance data from the official Bangladesh medical device database. Pure Global AI offers free access to Bangladesh DGDA's medical device registry, helping global MedTech companies navigate Bangladesh regulations efficiently.

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