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MEDICARE Fluid Warmer - Indonesia BPOM Medical Device Registration

MEDICARE Fluid Warmer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209918271. The device is manufactured by KEEWELL MEDICAL TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MITRA MEDITRANS INDONESIA.

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
MEDICARE Fluid Warmer
Analysis ID: AKL 20209918271

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MITRA MEDITRANS INDONESIA

AR Address

Jl Duri No. 2A jakarta Pusat

Registration Date

Oct 27, 2022

Expiry Date

May 10, 2027

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Blood and plasma warming device.

Non Radiation Electromedics

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