RUSCH Curved Reinforced Endotracheal Tube - Indonesia BPOM Medical Device Registration
RUSCH Curved Reinforced Endotracheal Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420327. 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. TELEFLEX MEDICAL INDONESIA.
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
Manufacturer
TELEFLEX MEDICAL SDN. BHD.Country of Origin
Malaysia
Authorized Representative
PT. TELEFLEX MEDICAL INDONESIAAR Address
Wisma 46 - Kota BNI Lantai 47, Units 01-04, Jl. Jend. Sudirman Kav. 1
Registration Date
May 16, 2024
Expiry Date
Nov 14, 2028
Product Type
Therapeutic Anesthesia Equipment
Tracheal tube.
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