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FEATHER Microtome Blade N35 - Indonesia BPOM Medical Device Registration

FEATHER Microtome Blade N35 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203810906. The device is manufactured by FEATHER SAFETY RAZOR CO.LTD. from Japan, 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
FEATHER Microtome Blade N35
Analysis ID: AKL 10203810906

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

PT. MIDIF FARMA

AR Address

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

Registration Date

Oct 25, 2024

Expiry Date

Dec 31, 2026

Product Type

Pathology Equipment and Accessories

Tissue processing equipment

Invitro Diagnostics

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