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PRO HISTO Embeding Casette - Indonesia BPOM Medical Device Registration

PRO HISTO Embeding Casette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203916333. The device is manufactured by CITOTEST LABWARE MANUFACTURING CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MIDIF FARMA.

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
PRO HISTO Embeding Casette
Analysis ID: AKL 10203916333

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. MIDIF FARMA

AR Address

Komplek Amarapura Blok E3 No.10 RT.001 Rw.005 Kel.Kademangan Kec.Setu

Registration Date

Mar 13, 2021

Expiry Date

Mar 10, 2024

Product Type

Pathology Equipment and Accessories

Tissue processing equipment (miscellaneous)

Invitro Diagnostics

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