Pure Global

Sodium Bicarbonate for haemodialysis (Bibag 5008) - FDA Registration 5552949d9e3129fa2394f69e080933ce

Access comprehensive regulatory information for Sodium Bicarbonate for haemodialysis (Bibag 5008) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5552949d9e3129fa2394f69e080933ce and manufactured by Fresenius Medical Care SMAD. The device was registered on May 27, 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.

Free Database
Powered by Pure Global AI
FDA Official Data
5552949d9e3129fa2394f69e080933ce
Sodium Bicarbonate for haemodialysis (Bibag 5008)
FDA ID: 5552949d9e3129fa2394f69e080933ce
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
Fresenius Medical Care
Registration Information
Analysis ID
5552949d9e3129fa2394f69e080933ce
Registration Date
May 27, 2022