GIBECK Humid-Vent Filter Pedi - Indonesia BPOM Medical Device Registration
GIBECK Humid-Vent Filter Pedi is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220920. The device is manufactured by TELEFLEX MEDICAL SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TELEFLEX MEDICAL SDN. BHD.Country of Origin
Malaysia
Authorized Representative
PT. MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Dec 07, 2022
Expiry Date
Dec 31, 2026
Product Type
Therapeutic Anesthesia Equipment
Breathing circuit bacterial filter.
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