MOYUUM Silicone Teether - Indonesia BPOM Medical Device Registration
MOYUUM Silicone Teether is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10604420099. The device is manufactured by SHINSUNG SILICONE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TIGASATU MEDIKA SOLUSINDO.
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 : 1
Manufacturer
SHINSUNG SILICONE CO., LTD.Country of Origin
Korea
Authorized Representative
PT. TIGASATU MEDIKA SOLUSINDOAR Address
Karawaci Office Park, Jalan Imam Bonjol, Ruko Finangsia Blok H 53, Prov. Banten, Kota Tangerang, Kec. Cibodas, Kel. Panunggangan Barat
Registration Date
Oct 25, 2024
Expiry Date
Jun 24, 2029
Product Type
Therapeutic Dental Equipment
Teething ring.
Non Electromedic Non Sterile
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