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CliniMACS PBS/EDTA Buffer - Indonesia BPOM Medical Device Registration

CliniMACS PBS/EDTA Buffer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320632. The device is manufactured by MILTENYI BIOTEC B.V. & CO. KG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOSAINS MEDIKA 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
CliniMACS PBS/EDTA Buffer
Analysis ID: AKL 20209320632

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. BIOSAINS MEDIKA INDONESIA

AR Address

PLAZA KARINDA BLOK B1/4, JALAN KARANG TENGAH RAYA

Registration Date

Sep 14, 2023

Expiry Date

Jan 01, 2027

Product Type

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

Automated blood cell separator

Invitro Diagnostics

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