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KIWI Omni-C Cup Vacuum Delivery System - Indonesia BPOM Medical Device Registration

KIWI Omni-C Cup Vacuum Delivery System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104903949. The device is manufactured by CLINICAL INNOVATIONS, LLC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.

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 : C
KIWI Omni-C Cup Vacuum Delivery System
Analysis ID: AKL 21104903949

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. TRANSMEDIC INDONESIA

AR Address

PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137

Registration Date

Aug 06, 2020

Expiry Date

Jun 09, 2025

Product Type

Surgical Obstetric and Gynaecological Equipment

Fetal vacuum extractor.

Non Electromedic Sterile

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