EMOS Laryngoscope - Indonesia BPOM Medical Device Registration
EMOS Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801120979. The device is manufactured by EMOS TECHNOLOGY GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRIADI LINTAS PERSADA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EMOS TECHNOLOGY GMBHCountry of Origin
Germany
Authorized Representative
TRIADI LINTAS PERSADAAR Address
Ruko Exclusive Raden Inten Jl. Raden Inten II No. 80 Kav. 5
Registration Date
Apr 18, 2023
Expiry Date
Apr 01, 2026
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
Non Electromedic Non Sterile
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