ORDISI Portable Suction Pump - Indonesia BPOM Medical Device Registration
ORDISI Portable Suction Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603213181. The device is manufactured by ORDISI S.A. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MANDIRI JAYA MEDIKA.
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
ORDISI S.A.Country of Origin
Spain
Authorized Representative
PT. MANDIRI JAYA MEDIKAAR Address
Graha Mas Fatmawati Blok B No. 20, Jl. RS. Fatmawati No. 71
Registration Date
Feb 10, 2020
Expiry Date
Sep 07, 2024
Product Type
Surgical Equipment
Powered suction pump.
Non Radiation Electromedics
EMA-LED Surgical Light
EMA-LED GMBH.
EMA-LED Surgical Light
EMA-LED GMBH.
EMALED Surgical Light
EMA-LED GMBH.
EMALED Operating Lamp
EMA-LED GMBH.
PERFORMANCE ICU Lung Fan
LEISTUNG EQUIPMENT LTDA.
HENNISS Cataract Instrument Set
A. HENNISS
PIGEON BUBBLE CPAP AD II
GUANGDONG PIGEON MEDICAL APPARATUS CO., LTD.
SONOSCANNER Ultrasound Scanner
SONOSCANNER SARL
PIGEON INFANT RESUSCITATION
GUANGDONG PIGEON MEDICAL APPARATUS CO., LTD.
PIGEON BUBBLE CPAP AD-I
GUANGDONG PIGEON MEDICAL APPARATUS CO., LTD.