VIVO Ultra Thin - Indonesia BPOM Medical Device Registration
VIVO Ultra Thin is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104520041. 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
KAREX INDUSTRIES SDN., BHD.Country of Origin
Malaysia
Authorized Representative
PT. DANPAC PHARMAAR 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 24, 2025
Expiry Date
Jan 23, 2028
Product Type
Therapeutic Obstetric and Gynecological Equipment
Condom.
Non Electromedic Non Sterile
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