RESTORATION ANATÓMICO
Mexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·STRYKER MÉXICO, S.A. DE C.V.·Registered August 02, 2018EL DISPOSITIVO RESTORATION ANATÓMICO ESTÁ INDICADO PARA SER UTILIZADO EN: - ENFERMEDAD ARTICULAR DOLOROSA, INCAPACITANTE, DE LA CADERA, RESULTANTE DE ARTRITIS DEGENERANTE, ARTRITIS REUMATOIDE, ARTRITIS POSTRAUMÁTICA O NECROSIS AVASCULAR AVANZADA. - REVI
THE ANATOMICAL RESTORATION DEVICE IS INDICATED FOR USE IN: - PAINFUL, DISABLING JOINT DISEASE OF THE HIP, RESULTING FROM DEGENERATING ARTHRITIS, RHEUMATOID ARTHRITIS, POST-TRAUMATIC ARTHRITIS OR ADVANCED AVASCULAR NECROSIS. - REVI
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
- Product Type (English)
- II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
- Trade Name (Spanish)
- SISTEMA DE COMPONENTE ACETABULAR
- Trade Name (English)
- ACETABULAR COMPONENT SYSTEM
- Analysis ID
- 1867C2018 SSA
- Registration Date
- August 02, 2018
- Name (Spanish)
- STRYKER MÉXICO, S.A. DE C.V.
- Name (English)
- STRYKER MEXICO, S.A. DE C.V.
Access comprehensive regulatory information for RESTORATION ANATÓMICO (ANATOMICAL RESTORATION) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1867C2018 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on August 02, 2018.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.