COLOPLAST OSTOMY POWDER - Indonesia BPOM Medical Device Registration
COLOPLAST OSTOMY POWDER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10805220504. The device is manufactured by COLOPLAST A/S from Denmark, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DCH AURIGA INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
COLOPLAST A/SCountry of Origin
Denmark
Authorized Representative
PT. DCH AURIGA INDONESIAAR Address
DCH AURIGA INDONESIA
Registration Date
Dec 22, 2022
Expiry Date
Sep 12, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Ostomy pouch and accessories.
Non Electromedic Non Sterile
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