Pure Global

The UNFOLDER Platinum 1 Series Cartridges - FDA Registration 7870f486824ed794e16652f14af8bd04

Access comprehensive regulatory information for The UNFOLDER Platinum 1 Series Cartridges in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7870f486824ed794e16652f14af8bd04 and manufactured by AMO Puerto Rico Manufacturing, Inc.. The device was registered on May 24, 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
7870f486824ed794e16652f14af8bd04
The UNFOLDER Platinum 1 Series Cartridges
FDA ID: 7870f486824ed794e16652f14af8bd04
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
Johnson & Johnson Vision
Registration Information
Analysis ID
7870f486824ed794e16652f14af8bd04
Registration Date
May 24, 2022
Authorized Representative