XTRA ™ Procedure Set - Indonesia BPOM Medical Device Registration
XTRA ™ Procedure Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321043. The device is manufactured by SORIN GROUP ITALIA S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS 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
SORIN GROUP ITALIA S.R.L.Country of Origin
Italy
Authorized Representative
PT. IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Nov 02, 2023
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Autotransfusion apparatus.
Non Electromedic Sterile
PORTEX Polar Preformed Tracheal Tube
SMITHS HEALTHCARE MANUFACTURING SA DE CV.
PORTEX BLUSELECT Suctionaid Tracheostomy Tube
SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V
PORTEX® Endobronchial Double Lumen
SMITHS HEALTHCARE MANUFACTURING SA DE C.V.
CADD 250 ml Medication Cassette Reservoirs
SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.
CADD Cassette Reservoirs-Non Flow Stop
SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.
PORTEX BLUSELECT Tracheostomy Tube (Uncuffed)
SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V
PORTEX Nasopharyngeal Airway
SMITHS HEALTHCARE MANUFACTURING SA DE C.V.
MINFOUND PET and Computed Tomography System
MINFOUND MEDICAL SYSTEMS CO. LTD.
LAERDAL BaXstrap Spineboard
FORMED PLASTICS INC.
BAXTER Ceiling-Mounted Support System
BAXTER MEDICAL SYSTEMS GMBH+ CO. KG.,