Pure Global

TSK CHIBA Biopsy Needle - Indonesia BPOM Medical Device Registration

TSK CHIBA Biopsy Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801610304. The device is manufactured by TSK LABORATORY, JAPAN SOJA NO. 1 FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NATURAL HILIFE.

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 : B
TSK CHIBA Biopsy Needle
Analysis ID: AKL 20801610304

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. NATURAL HILIFE

AR Address

JL. TENTARA PELAJAR 112 RT 07/05 KEL. KEMIRIREJO, KEC. MAGELANG TENGAH, KOTA MAGELANG, JAWA TENGAH

Registration Date

May 16, 2023

Expiry Date

Mar 31, 2027

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from TSK LABORATORY, JAPAN SOJA NO. 1 FACTORY
Products from the same manufacturer (3 products)