FENTEX SURGICAL Laryngoscope - Indonesia BPOM Medical Device Registration
FENTEX SURGICAL Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403220350. The device is manufactured by FENTEX SURGICAL INSTRUMENTS from Pakistan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDMAX GLOBAL INDOTAMA.
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
Manufacturer
FENTEX SURGICAL INSTRUMENTSCountry of Origin
Pakistan
Authorized Representative
PT. MEDMAX GLOBAL INDOTAMAAR Address
Perum Taman Candiloka C3-7 Ngampelsari Candi Sidoarjo
Registration Date
Jun 13, 2022
Expiry Date
May 30, 2026
Product Type
Therapeutic Anesthesia Equipment
Rigid laryngoscope.
Non Electromedic Non Sterile
CREATE BIOTECH NIV Mask
CREATE BIOTECH CO., LTD.
CREATE Biotech Nebulizer Kit
CREATE BIOTECH CO., LTD.
CREATE BIOTECH Flow Sensor Breating Circuit
CREATE BIOTECH CO., LTD.
CREATE BIOTECH Anesthetic Gas Mask
CREATE BIOTECH CO., LTD.
CREATE BIOTECH Mapleson Breathing Circuit
CREATE BIOTECH CO., LTD.
Create Biotech Breathing System Filter
CREATE BIOTECH CO., LTD.
CREATE BIOTECH Breathing Circuit and Accessories
CREATE BIOTECH CO., LTD.
CREATE BIOTECH Laryngeal Mask Airway Double-Lumen
CREATE BIOTECH CO., LTD.
CREATE BIOTECH Closed Suction Catheter
CREATE BIOTECH CO., LTD.
CREATE BiIOTECH Reusable Breathing Circuit and Accessories
CREATE BIOTECH CO., LTD.