HUDSON RCI Sheridan Sher-I-Bronch - Indonesia BPOM Medical Device Registration
HUDSON RCI Sheridan Sher-I-Bronch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403211518. The device is manufactured by TELEFLEX MEDICAL. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TELEFLEX MEDICAL.Country of Origin
Mexico
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Nov 01, 2021
Expiry Date
Dec 31, 2023
Product Type
Therapeutic Anesthesia Equipment
Bronchial tube.
Non Electromedic Sterile
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