BICAKCILAR Tracheal Tube Murphy - Indonesia BPOM Medical Device Registration
BICAKCILAR Tracheal Tube Murphy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403210474. The device is manufactured by BIรAKCILAR TIBBI CIHAZLAR SANAYI VE TICARET A.S. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Country of Origin
Turkey
Authorized Representative
PT. SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Nov 17, 2023
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Tracheal tube.
Non Electromedic Sterile
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BICAKCILAR Tracheal Tube Murphy
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