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KLF Plasma Freezer 12-18 - Indonesia BPOM Medical Device Registration

KLF Plasma Freezer 12-18 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209023930. The device is manufactured by CRYO LIFE SCIENCE TECHNOLOGIES GMBH from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIMA ALKESINDO NUSANTARA.

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
KLF Plasma Freezer 12-18
Analysis ID: AKL 20209023930

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Austria

Authorized Representative

PT. PRIMA ALKESINDO NUSANTARA

AR Address

Jl. Bukit Gading Raya Blok C 12 - C 15 Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara

Registration Date

Jul 14, 2020

Expiry Date

Jun 01, 2024

Product Type

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

Processing system for frozen blood.

Invitro Diagnostics

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