GEA Ultrasound Gel - Indonesia BPOM Medical Device Registration
GEA Ultrasound Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903221550. The device is manufactured by SKYLER BIOTECH SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SKYLER BIOTECH SDN. BHD.Country of Origin
Malaysia
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Jan 25, 2023
Expiry Date
Sep 01, 2025
Product Type
General Hospital Equipment and Other Individuals
Patient lubricant.
Non Electromedic Non Sterile
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