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GelPOINT V-Path Transvaginal Access Platform - Indonesia BPOM Medical Device Registration

GelPOINT V-Path Transvaginal Access Platform is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106520011. The device is manufactured by APPLIED MEDICAL RESOURCES CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BRIDGE TWO.

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 : B
GelPOINT V-Path Transvaginal Access Platform
Analysis ID: AKL 21106520011

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Feb 03, 2025

Expiry Date

Dec 31, 2026

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Culdoscope and accessories.

Non Electromedic Sterile

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