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BOSKA Infusion Pump - Indonesia BPOM Medical Device Registration

BOSKA Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902322173. The device is manufactured by BEIJING KELLYMED, CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. 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 : B
BOSKA Infusion Pump
Analysis ID: AKL 20902322173

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. KARUNIAJAYA ANDALAN PRIMA

AR Address

RUKO JALUR SUTERA TIMUR BLOK. 6B NO. 23 ALAM SUTERA, SERPONG, TANGERANG 15144.

Registration Date

Jun 11, 2023

Expiry Date

May 18, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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