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BOSKA Patient Monitor 12 Inch - Indonesia BPOM Medical Device Registration

BOSKA Patient Monitor 12 Inch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420268. The device is manufactured by SHENZHEN LE MEDICAL TECHNOLOGY , CO, LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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 : B
BOSKA Patient Monitor 12 Inch
Analysis ID: AKL 20502420268

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

KARUNIAJAYA ANDALAN PRIMA

AR Address

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

Registration Date

Aug 04, 2024

Expiry Date

Aug 02, 2027

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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