SUMI Nasopharyngeal Airway - Indonesia BPOM Medical Device Registration
SUMI Nasopharyngeal Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10401111392. The device is manufactured by SUMI SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ SP. K. from Poland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is 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 : 1
Country of Origin
Poland
Authorized Representative
SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Dec 08, 2022
Expiry Date
Nov 04, 2025
Product Type
Therapeutic Anesthesia Equipment
Nasopharyngeal airway
Non Electromedic Sterile
IDRA – Dedicated Dry Eye Platform
SBM SISTEMI S. R. L
SBM DSLC 200
SBM SISTEMI S.R.L.
SBM DEM 100
SBM SISTEMI S.R.L.
LUMENIS Digital OptiLight System
LUMENIS BE INC.
PLASMAGE
BRERA MEDICAL TECHNOLOGIES S.R.L
LITHOTRIPTER 3000 Plus
RICHARD WOLF GMBH
UFSK Surgeon's Chair surgiForce Light, with Formed Seat
UFSK-INTERNATIONAL OSYS GMBH
LUMENIS Pulse 120H, Moses 2.0
LUMENIS LTD.
MEDTRON ACCUTRON MR
MEDTRON AG.
VERSIUS Surgical System with vLimelite
CMR SURGICAL LIMITED