PTH (1-84) ROCHE
PRUEBA INMUNOLÓGICA IN VITRO PARA LADETERMINACIÓN CUANTITATIVA DE LA HORMONAPARATIROIDEABIOINTACTA(PTH1‑84)ENSUEROYPLASMAHUMANOSENLOSINMUNOANALIZADORESROCHE.AGENTEDEDIAGNÓSTICOPARAUSOINVITRO.PARAUSOEXCLUSIVODE LABORATORIOS
IN VITRO IMMUNOLOGICAL TEST FOR QUANTITATIVE DETERMINATION OF BIOINTACT PARATHYROID HORMONE (PTH1-84) IN HUMAN SERUM AND PLASMA IN RESROCHE IMMUNOASSAYS. DIAGNOSTIC AGENTFOR use. FOR THE EXCLUSIVE USE OF LABORATORIES
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA PARA LADETERMINACIÓN DE LAHORMONA PARATIROIDEAINTACTA (PTH 1-84)
- Trade Name (English)
- TEST FOR INTACT PARATHYROID HORMONE (PTH 1-84)
- Analysis ID
- 0989R2022 SSA
- Registration Date
- September 27, 2022
- Name (Spanish)
- PRODUCTOSROCHE, S.A. DE C.V.
- Name (English)
- PRODUCTOSROCHE, S.A. DE C.V.
Access comprehensive regulatory information for PTH (1-84) ROCHE (PTH (1-84) ROCK) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0989R2022 SSA and manufactured by PRODUCTOSROCHE, S.A. DE C.V.. The device was registered on September 27, 2022.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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.