Pure Global

VERSACUT Tissue Morcellator - Indonesia BPOM Medical Device Registration

VERSACUT Tissue Morcellator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804220181. The device is manufactured by LUMENIS LTD. from Israel, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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
VERSACUT Tissue Morcellator
Analysis ID: AKL 20804220181

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

LUMENIS LTD.

Country of Origin

Israel

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Jul 29, 2024

Expiry Date

Sep 30, 2025

Product Type

Gastroenterology-Surgical Urology Equipment

Endoscopic electrosurgical unit and accessories.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from LUMENIS LTD.
Products from the same manufacturer (2 products)