MEROCEL - Indonesia BPOM Medical Device Registration
MEROCEL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703915886. The device is manufactured by MEDTRONIC XOMED, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MEDTRONIC XOMED, INC.Country of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama
Registration Date
Aug 11, 2023
Expiry Date
Feb 07, 2028
Product Type
Ear, Nose and Throat Surgical Equipment
Intranasal splint.
Non Electromedic Sterile
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