BruiseMD™ Gel - Indonesia BPOM Medical Device Registration
BruiseMD™ Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603125329. The device is manufactured by NEFTIS LABORATORIES. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REDO MARKETING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NEFTIS LABORATORIES.Country of Origin
Spain
Authorized Representative
PT. REDO MARKETING INDONESIAAR Address
Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang
Registration Date
Sep 03, 2021
Expiry Date
Jul 07, 2026
Product Type
Surgical Equipment
Hydrogel wound dressing and burn dressing.
Non Electromedic Non Sterile
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