Mexico COFEPRIS registration 1347C2024 SSA
APÓSITO
EN: APÓSITO
Device classification
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- V. Materiales quirúrgicos y de curación
- Product Type (English)
- V. Materiales quirúrgicos y de curación
- Trade Name (Spanish)
- POLYMEM®
- Trade Name (English)
- POLYMEM®
Registration information
- Analysis ID
- 1347C2024 SSA
- Registration Date
- May 09, 2024
Manufacturer / Fabricante
- Name (Spanish)
- EMERGO, S. DE R.L. DE C.V.
- Name (English)
- EMERGO, S. DE R.L. DE C.V.
About this record
Access comprehensive regulatory information for APÓSITO (APÓSITO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1347C2024 SSA and manufactured by EMERGO, S. DE R.L. DE C.V.. The device was registered on May 09, 2024.
This page provides complete registration details including product type (V. Materiales quirúrgicos y de curación), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
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