DIROS OWL DXE Cannula - Indonesia BPOM Medical Device Registration
DIROS OWL DXE Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002812364. The device is manufactured by DIROS TECHNOLOGY INC. from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SCHMIDT BIOMEDTECH INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIROS TECHNOLOGY INC.Country of Origin
Canada
Authorized Representative
PT. SCHMIDT BIOMEDTECH INDONESIAAR Address
Gading Riverview Blok H-52 Jl. Mall of Indonesia Gate
Registration Date
Dec 05, 2021
Expiry Date
Dec 31, 2023
Product Type
Surgical Neurology Equipment
Radiofrequency lesion probe.
Non Electromedic Sterile
