GIBECK Humid-Vent Filter - Indonesia BPOM Medical Device Registration
GIBECK Humid-Vent Filter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220959. 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
The Kensington Office Tower Lantai 11, Jalan Boulevard Raya Nomor 1, Desa/Kelurahan Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, 14240
Registration Date
Oct 27, 2023
Expiry Date
Dec 31, 2026
Product Type
Therapeutic Anesthesia Equipment
Breathing circuit bacterial filter.
Non Electromedic Non Sterile
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