Dermashine Pro - Indonesia BPOM Medical Device Registration
Dermashine Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903028254. The device is manufactured by PANACE CO.,LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SMELL MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PANACE CO.,LTD.Country of Origin
Korea
Authorized Representative
SMELL MEDICAL INDONESIAAR Address
Gd. Graha Mampang lt. 2. Jl. Mampang Prapatan Raya no. 100 Duren Tiga Pancoran
Registration Date
Dec 29, 2020
Expiry Date
Oct 23, 2025
Product Type
General Hospital Equipment and Other Individuals
Syringe needle introducer.
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