KAWE F.O Laryngoskop-Set Adults (REF. 03.62020.011) - Indonesia BPOM Medical Device Registration
KAWE F.O Laryngoskop-Set Adults (REF. 03.62020.011) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403812700. The device is manufactured by KAWE-KIRCHNER & WILHELM GMBH+CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. POLARIS ALKES STARINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
KAWE-KIRCHNER & WILHELM GMBH+CO., KG.Country of Origin
Germany
Authorized Representative
PT. POLARIS ALKES STARINDOAR Address
JL. Gunung Sahari Raya No. 12 G Gunung Sahari Utara, Sawah Besar
Registration Date
Sep 02, 2019
Expiry Date
Mar 25, 2024
Product Type
Therapeutic Anesthesia Equipment
Rigid laryngoscope.
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