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VIVO Bubble Gum Lube - Indonesia BPOM Medical Device Registration

VIVO Bubble Gum Lube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104520001. The device is manufactured by KAREX INDUSTRIES SDN., BHD from Malaysia, and is classified as Risk Class Kelas Resiko : B. 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 : B
VIVO Bubble Gum Lube
Analysis ID: AKL 21104520001

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. DANPAC PHARMA

AR Address

Green Sedayu Biz Park, Blok DM5, No. 31E, Jl. Daan Mogot, KM 18, RT.11/RW.6, Kelurahan Kalideres, Kecamatan Kalideres, Kota Jakarta Barat, Daerah Khusus Ibukota Jakarta 11840

Registration Date

Jan 03, 2025

Expiry Date

Jan 01, 2028

Product Type

Therapeutic Obstetric and Gynecological Equipment

Condom lubricant

Non Electromedic Non Sterile

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