BLOW 165 DUO - Indonesia BPOM Medical Device Registration
BLOW 165 DUO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801913340. The device is manufactured by PUFF from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is VERSACON MEDICAL.
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SOPRO 165 DUO
Risk Classification
Product Class
Kelas : 2
Manufacturer
PUFFCountry of Origin
France
Authorized Representative
VERSACON MEDICALAR Address
JL ANGGREK NELI MURNI BLOK C NO 30-30 A, PALMERAH
Registration Date
Jun 21, 2019
Expiry Date
Mar 25, 2024
Product Type
Diagnostic Gastroenterology-Urology Equipment
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