ULTRABRAID
Mexico·Clase III·V. SURGICAL AND HEALING MATERIALS·SMITH & NEPHEW, S.A. DE C.V.·Registered June 01, 2018LA SUTURA ULTRABRAID ESTÁ INDICADA PARA SU USO EN LA APROXIMACIÓN Y/O UNIÓN DE TEJIDOS BLANDOS, INCLUYENDO ALOINJERTOS PARA CIRUGÍAS ORTOPÉDICAS.
THE ULTRABRAID SUTURE IS INDICATED FOR USE IN THE APPROXIMATION AND/OR JOINING OF SOFT TISSUES, INCLUDING ALLOGRAFTS FOR ORTHOPEDIC SURGERIES.
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
- Product Type (English)
- V. SURGICAL AND HEALING MATERIALS
- Trade Name (Spanish)
- SUTURA QUIRÚRGICA NO ABSORBIBLE DE POLIETILENO DE ULTRA PESO MOLECULAR CON AGUJA.
- Trade Name (English)
- NON-ABSORBABLE SURGICAL SUTURE OF ULTRA MOLECULAR WEIGHT POLYETHYLENE WITH NEEDLE.
- Analysis ID
- 1303C2018 SSA
- Registration Date
- June 01, 2018
- Name (Spanish)
- SMITH & NEPHEW, S.A. DE C.V.
- Name (English)
- SMITH & NEPHEW, S.A. DE C.V.
Access comprehensive regulatory information for ULTRABRAID (ULTRABRAID) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1303C2018 SSA and manufactured by SMITH & NEPHEW, S.A. DE C.V.. The device was registered on June 01, 2018.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.