ANSPACH eMax 2 Plus Handpiece - Indonesia BPOM Medical Device Registration
ANSPACH eMax 2 Plus Handpiece is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11002320159. The device is manufactured by THE ANSPACH EFFORT, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is JOHNSON AND JOHNSON INDONESIA TWO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
THE ANSPACH EFFORT, INC.Country of Origin
United States
Authorized Representative
JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A, Kuningan, Setiabudi, Jakarta Selatan, Desa/Kelurahan Kuningan Timur, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12950
Registration Date
Jul 24, 2023
Expiry Date
Jan 10, 2028
Product Type
Surgical Neurology Equipment
Cranial drill handpiece (brace).
Non Electromedic Non Sterile
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