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HISTOLINE Manual Rotary Microtome MR2258 And Accessories - Indonesia BPOM Medical Device Registration

HISTOLINE Manual Rotary Microtome MR2258 And Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203811409. The device is manufactured by HISTOLINE LABORATORIE SRL. from Italy, 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
HISTOLINE Manual Rotary Microtome MR2258 And Accessories
Analysis ID: AKL 10203811409

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Italy

Authorized Representative

PT. MIDIF FARMA

AR Address

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

Registration Date

Nov 26, 2024

Expiry Date

Oct 15, 2029

Product Type

Pathology Equipment and Accessories

Tissue processing equipment

Invitro Diagnostics

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