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TREVO XP ProVue Retriever - Indonesia BPOM Medical Device Registration

TREVO XP ProVue Retriever is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501126999. 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 PT. WICAKSANA OVERSEAS INTERNATIONAL.

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.

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BPOM Registered
Risk Class Kelas Resiko : C
TREVO XP ProVue Retriever
Analysis ID: AKL 20501126999

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. WICAKSANA OVERSEAS INTERNATIONAL

AR Address

Jl. Ancol Barat VII Blok A5/D No. 2 RT 006 RW 001

Registration Date

May 10, 2023

Expiry Date

Jan 31, 2024

Product Type

Diagnostic Cardiology Equipment

Percutaneous catheter.

Non Electromedic Sterile

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