MORTON Reusable Rebreathing Bags - Indonesia BPOM Medical Device Registration
MORTON Reusable Rebreathing Bags is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403911818. The device is manufactured by MORTON MEDICAL SANAYI VE TIC., LTD., STI. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.
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
MORTON MEDICAL SANAYI VE TIC., LTD., STI.Country of Origin
Turkey
Authorized Representative
PT. ALKESTRON SELF-SOURCEAR Address
Komp Ruko Griya Inti Sentosa Jln. Griya Agung Blok O No. 95-96
Registration Date
Apr 16, 2019
Expiry Date
Mar 05, 2024
Product Type
Therapeutic Anesthesia Equipment
Rebreathing device.
Non Electromedic Non Sterile
MOTEX Surgical Gloves Lightly Powdered
SHANGHAI MOTEX HEALTHCARE CO., LTD.
NAFERN Soda Lime
SHANGHAI NAHUI DRYING REAGENT FACTORY
VENAR TS Anaesthesi Unit
CHIRANA MEDICAL, A.S.
PUREMEDIC Fetal Maternal/Monitor
SHENZEN JUMPER MEDICAL EQUIPMENT CO. LTD
PUREMEDIC Fetal Monitor
SHENZEN JUMPER MEDICAL EQUIPMENT CO. LTD
ASPEL Electrocardiograph
ASPEL S.A.
CARDIOMAX Defibrillator
INSTRAMED INDUSTRIA MEDICO HOSPITALAR LTDA.
BILICARE ™ Neonatal Noninvasive Bilirubin Meter
GERIUM MEDICAL LTD.
ELECTRO-MAG Microprocessor Water Bath
ELEKTRO-MAG LABORATUVAR ALETLERI SAN. VE TIC. A.S.
ELECTRO-MAG Incubator M 6040 BP
ELEKTRO-MAG LABORATUVAR ALETLERI SAN. VE TIC. AS.