Surfcath - Indonesia BPOM Medical Device Registration
Surfcath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324316. The device is manufactured by SIPV from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIPVCountry of Origin
France
Authorized Representative
IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Jun 23, 2023
Expiry Date
Dec 31, 2025
Product Type
Surgical Equipment
Introduction/drainage catheter and accessories.
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