A.M.I. HAL Instrument - Indonesia BPOM Medical Device Registration
A.M.I. HAL Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603313682. The device is manufactured by A.M.I. AGENCY FOR MEDICAL INNOVATIONS GMBH from Austria, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is DIAN LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
A.M.I. AGENCY FOR MEDICAL INNOVATIONS GMBHCountry of Origin
Austria
Authorized Representative
DIAN LANGGENG PRATAMAAR Address
Gedung Dinar, Jl. Raden Saleh Raya No. 4 RT.10/RW.01, Kel. Kenari, Kec. Senen. Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos 10430
Registration Date
May 04, 2023
Expiry Date
Dec 31, 2026
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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