CapnoPen CP-001k - Indonesia BPOM Medical Device Registration
CapnoPen CP-001k is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420284. The device is manufactured by CAPNOPHARM GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PACIFIC SAINTIFINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CAPNOPHARM GMBHCountry of Origin
Germany
Authorized Representative
PT. PACIFIC SAINTIFINDOAR Address
Komplek Green Lake City Rukan Crown Blok C nomor 27 RT 012 RW 011 Kel. Petir Kec. Cipondoh, Tangerang, Provinsi Banten 15147
Registration Date
Aug 01, 2024
Expiry Date
Jan 15, 2029
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
Non Electromedic Sterile
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