Pure Global

DORO® Non-Stick Bipolar Forceps - Indonesia BPOM Medical Device Registration

DORO® Non-Stick Bipolar Forceps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603022856. The device is manufactured by PRO MED INSTRUMENTS GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. 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 : C
DORO® Non-Stick Bipolar Forceps
Analysis ID: AKL 21603022856

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. OPMIC PERKASA MANDIRI

AR Address

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

Registration Date

Dec 04, 2021

Expiry Date

Feb 10, 2025

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing