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BOSKA Defibrillator Monitor - Indonesia BPOM Medical Device Registration

BOSKA Defibrillator Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505320258. The device is manufactured by AMBULANC (SHENZHEN) TECH. CO., LTD OGY CO. LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. KARUNIAJAYA ANDALAN PRIMA.

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 : D
BOSKA Defibrillator Monitor
Analysis ID: AKL 30505320258

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. KARUNIAJAYA ANDALAN PRIMA

AR Address

Ruko Jalur Sutera Timur 6B No. 23, Alam Sutera , RT.01/RW.15

Registration Date

Aug 15, 2023

Expiry Date

Aug 13, 2026

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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