PLASTI-MED Breathing Circuit - Smoothbore - Indonesia BPOM Medical Device Registration
PLASTI-MED Breathing Circuit - Smoothbore is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403220310. The device is manufactured by PLASTI-MED PLASTIC MEDICAL URUNLER SAN. TIC. LTD. ST. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. EDISON AMBASSADOR MEANS.
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Risk Classification
Product Class
Kelas : 1
Country of Origin
Turkey
Authorized Representative
PT. EDISON AMBASSADOR MEANSAR Address
Jl. Oasis Sememi Raya No. 1 RT 05 RW 04, Kel. Sememi, Kec. Benowo, Surabaya, Jawa Timur
Registration Date
Feb 05, 2024
Expiry Date
Dec 08, 2027
Product Type
Therapeutic Anesthesia Equipment
Anesthesia breathing circuit.
Non Electromedic Non Sterile
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