MORTON Jackson Rees System - Indonesia BPOM Medical Device Registration
MORTON Jackson Rees System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403510777. The device is manufactured by MORTON MEDIKAL SAN. VE TIC A.S. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MORTON MEDIKAL SAN. VE TIC A.S.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
May 27, 2019
Expiry Date
Mar 05, 2024
Product Type
Therapeutic Anesthesia Equipment
Anesthesia breathing circuit.
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