PRUEBA RÁPIDA PARA LA DETECCIÓN CUALITATIVA DE LA GONADOTROPINA CORIÓNICA HUMANA (HCG)
Mexico·Clase I·III. Agentes de diagnóstico·LAB-CENTER DE
MÉXICO S.A. DE C.V.·Registered October 28, 2022- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- SPINCARD HCG
- Trade Name (English)
- SPINCARD HCG
- Analysis ID
- 1237R2022 SSA
- Registration Date
- October 28, 2022
- Name (Spanish)
- LAB-CENTER DE MÉXICO S.A. DE C.V.
- Name (English)
- LAB-CENTER DE MÉXICO S.A. DE C.V.
Access comprehensive regulatory information for PRUEBA RÁPIDA PARA LA DETECCIÓN CUALITATIVA DE LA GONADOTROPINA CORIÓNICA HUMANA (HCG) (PRUEBA RÁPIDA PARA LA DETECCIÓN CUALITATIVA DE LA GONADOTROPINA CORIÓNICA HUMANA (HCG)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1237R2022 SSA and manufactured by LAB-CENTER DE MÉXICO S.A. DE C.V.. The device was registered on October 28, 2022.
This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.