GUIDESTAR STEERABLE GUIDING SHEATH - Indonesia BPOM Medical Device Registration
GUIDESTAR STEERABLE GUIDING SHEATH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320724. The device is manufactured by OSCOR CARIBE LLC from Dominican, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JOHNSON AND JOHNSON INDONESIA 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
OSCOR CARIBE LLCCountry of Origin
Dominican
Authorized Representative
PT. JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A, Kuningan, Setiabudi, Jakarta Selatan, Desa/Kelurahan Kuningan Timur, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12950
Registration Date
May 07, 2023
Expiry Date
Dec 30, 2027
Product Type
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