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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 20501126587. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
TREVO Pro Microcatheter
Analysis ID: AKL 20501126587

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 A 5D No. 2 RT.006/RW.001, Kel. Ancol, Kec. Pademangan, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta

Registration Date

May 16, 2023

Expiry Date

Jan 31, 2024

Product Type

Diagnostic Cardiology Equipment

Continuous flush catheter.

Non Electromedic Sterile

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