RUSCH – Crystal Clear Tracheostomy Cannula - Indonesia BPOM Medical Device Registration
RUSCH – Crystal Clear Tracheostomy Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403914097. 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. LABORA MANDIRI INDO PRATAMA.
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 BHDCountry of Origin
Malaysia
Authorized Representative
PT. LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47
Registration Date
Oct 14, 2021
Expiry Date
Dec 31, 2023
Product Type
Therapeutic Anesthesia Equipment
Tracheostomy tube and tube cuff.
Non Electromedic Sterile
VITREX SOFT Sterile Blood Lancets
STERILANCE MEDICAL (SUZHOU) INC.
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