Pure Global

GEOTEK Semi-Automatic Biopsy Needle - Indonesia BPOM Medical Device Registration

GEOTEK Semi-Automatic Biopsy Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801026599. The device is manufactured by GEOTEK MEDIKAL VE SAGLIK HIZMETLERI TIC. SAN. LTD. ลžTI from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ABADINUSA USAHASEMESTA.

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 : C
GEOTEK Semi-Automatic Biopsy Needle
Analysis ID: AKL 20801026599

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. ABADINUSA USAHASEMESTA

AR Address

Jalan Raden Saleh No. 45 G

Registration Date

Nov 04, 2020

Expiry Date

Mar 05, 2024

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument (electric)

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing