3M™ Cavilon™ Durable Barrier Cream - Indonesia BPOM Medical Device Registration
3M™ Cavilon™ Durable Barrier Cream is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902127040. The device is manufactured by ACCUPAC, LLC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 3M INDONESIA IMPORTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACCUPAC, LLCCountry of Origin
United States
Authorized Representative
3M INDONESIA IMPORTAMAAR Address
KAWASAN PERKANTORAN HIJAU ARKADIA, TOWER F, LT.9, JL. TB. SIMATUPANG KAV. 88
Registration Date
Nov 17, 2021
Expiry Date
Sep 10, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Liquid bandage.
Non Electromedic Non Sterile
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