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TOSOH AIA-PACK Folate Pretreatment Set - Indonesia BPOM Medical Device Registration

TOSOH AIA-PACK Folate Pretreatment Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204210577. The device is manufactured by TOSOH AIA, INC. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is KARINDO ALKESTRON.

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 : A
TOSOH AIA-PACK Folate Pretreatment Set
Analysis ID: AKL 10204210577

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

TOSOH AIA, INC.

Country of Origin

Japan

Authorized Representative

KARINDO ALKESTRON

AR Address

JL. TOMANG RAYA NO.17

Registration Date

Jan 24, 2022

Expiry Date

Aug 31, 2026

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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