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SENSITIF VIVO Ultra Thin - Indonesia BPOM Medical Device Registration

SENSITIF VIVO Ultra Thin is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104220099. The device is manufactured by KAREX INDUSTRIES SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DANPAC PHARMA.

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
SENSITIF VIVO Ultra Thin
Analysis ID: AKL 21104220099

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. DANPAC PHARMA

AR Address

Plaza Asia, Lt. 6D, Kav. 59, RT 005/RW 003

Registration Date

Apr 19, 2022

Expiry Date

Apr 18, 2025

Product Type

Therapeutic Obstetric and Gynecological Equipment

Condom.

Non Electromedic Non Sterile

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