Pure Global

Intraocular Lens - FDA Registration 390f17bfa9ec62b7c0a7392eff69b764

Access comprehensive regulatory information for Intraocular Lens in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 390f17bfa9ec62b7c0a7392eff69b764 and manufactured by Carl Zeiss Meditec S.A.S. The device was registered on July 06, 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
390f17bfa9ec62b7c0a7392eff69b764
Intraocular Lens
FDA ID: 390f17bfa9ec62b7c0a7392eff69b764
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
Zeiss
Registration Information
Analysis ID
390f17bfa9ec62b7c0a7392eff69b764
Registration Date
July 06, 2022
Manufacturer
Authorized Representative