TREVO Pro Microcatheter - Indonesia BPOM Medical Device Registration
TREVO Pro Microcatheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420086. The device is manufactured by STRYKER NEUROVASCULAR from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is NUGRA KARSERA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
STRYKER NEUROVASCULARCountry of Origin
United States
Authorized Representative
NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Feb 17, 2024
Expiry Date
Jun 30, 2025
Product Type
Diagnostic Cardiology Equipment
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