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DORATEK Microfacture Treatment System - Indonesia BPOM Medical Device Registration

DORATEK Microfacture Treatment System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303917219. The device is manufactured by DORATEK MEDIKAL ELEKTRIK MAKINA IMALATI TURIZM INSAAT SANAYI VE LTD. STI from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. EUPHRATES WITH.

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
DORATEK Microfacture Treatment System
Analysis ID: AKL 11303917219

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Turkey

Authorized Representative

PT. EUPHRATES WITH

AR Address

Ruko Gardenia kav 1, jln. parigi raya no 75 sukabakti curug 15810

Registration Date

Nov 05, 2019

Expiry Date

Mar 17, 2024

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Sterile

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