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SZMIC Plasma Thawer KJX-IA - Indonesia BPOM Medical Device Registration

SZMIC Plasma Thawer KJX-IA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209802439. The device is manufactured by SUZHOU MEDICAL INSTRUMENTS FACTORY. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ABHIMATA MANUNGGAL.

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
SZMIC Plasma Thawer KJX-IA
Analysis ID: AKL 20209802439

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ABHIMATA MANUNGGAL

AR Address

Jl. Perniagaan Timur No. 27, Desa/Kelurahan Roa Malaka, Kec. Tambora, Kota Adm. Jakarta Barat, Provinsi DKI Jakarta, Kode Pos 11230

Registration Date

Jun 16, 2023

Expiry Date

Jul 19, 2028

Product Type

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

Blood and plasma warming device.

Invitro Diagnostics

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