RUSCH EZ-Blocker Kit - Indonesia BPOM Medical Device Registration
RUSCH EZ-Blocker Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420186. The device is manufactured by ARROW INTERNATIONAL CR, A.S. from Czech Republic, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TELEFLEX MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ARROW INTERNATIONAL CR, A.S.Country of Origin
Czech Republic
Authorized Representative
PT. TELEFLEX MEDICAL INDONESIAAR Address
Wisma 46 - Kota BNI Lantai 47, Units 01-04, Jl. Jend. Sudirman Kav. 1
Registration Date
Aug 26, 2024
Expiry Date
Nov 14, 2028
Product Type
Therapeutic Anesthesia Equipment
Tracheal/bronchial differential ventilation tube.
Non Electromedic Sterile
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