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enShock - Indonesia BPOM Medical Device Registration

enShock is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403420204. The device is manufactured by REMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SURYA TAMA MEDIKA.

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
enShock
Analysis ID: AKL 21403420204

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

REMED CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. SURYA TAMA MEDIKA

AR Address

Jl m hasibuan ruko suncity pbb. 37 real blok e.27 rt 004 rw 002 kel margajaya kec bekasi selatan kota bekasi

Registration Date

May 31, 2024

Expiry Date

Jul 28, 2026

Product Type

Therapeutic Physical Health Equipment

Extracorporeal shock wave treatment device

Non Radiation Electromedics

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