PUTTI ATTI Teether - Indonesia BPOM Medical Device Registration
PUTTI ATTI Teether is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10604812332. The device is manufactured by LEE & LEE HI-TECH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LEE & LEE HI-TECH CO., LTD.Country of Origin
Korea
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Mar 02, 2023
Expiry Date
Apr 20, 2024
Product Type
Therapeutic Dental Equipment
Teething ring.
Non Electromedic Non Sterile
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