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KANMED Baby Warmer - Indonesia BPOM Medical Device Registration

KANMED Baby Warmer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902111413. The device is manufactured by KANMED. from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CITRA VITA BUANA.

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
KANMED Baby Warmer
Analysis ID: AKL 20902111413

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

KANMED.

Country of Origin

Sweden

Authorized Representative

PT. CITRA VITA BUANA

AR Address

Jl. M. Hasibuan, Ruko Suncity Square Blok E-18 RT 004 RW 002

Registration Date

Jul 22, 2022

Expiry Date

Dec 31, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Infant radiant warmer.

Non Radiation Electromedics

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