Pure Global

TAKAYAMA Microsurgical Titanium Instrumen - Indonesia BPOM Medical Device Registration

TAKAYAMA Microsurgical Titanium Instrumen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11002320170. The device is manufactured by TAKAYAMA INSTRUMENT INC. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. OPMIC PERKASA MANDIRI.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
TAKAYAMA Microsurgical Titanium Instrumen
Analysis ID: AKL 11002320170

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

PT. OPMIC PERKASA MANDIRI

AR Address

Jl.Puri Kencana Blok K7-3D 3rd Fl Kembangan Jakarta 11610

Registration Date

Aug 23, 2023

Expiry Date

Feb 13, 2028

Product Type

Surgical Neurology Equipment

Microsurgical instrument.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from TAKAYAMA INSTRUMENT INC.
Products from the same manufacturer (1 products)