3M ESPE FILTEK Bulk Fill Flowable Restorative - Indonesia BPOM Medical Device Registration
3M ESPE FILTEK Bulk Fill Flowable Restorative is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420172. The device is manufactured by 3M ESPE DENTAL PRODUCTS from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is COBRA DENTAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
3M ESPE DENTAL PRODUCTSCountry of Origin
United States
Authorized Representative
COBRA DENTAL INDONESIAAR Address
Jl. Pakuningratan No. 69
Registration Date
Apr 16, 2024
Expiry Date
Aug 28, 2028
Product Type
Prosthetic Dental Equipment
Tooth shade resin material.
Non Electromedic Non Sterile
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