TRULIFE Pressure Care - Indonesia BPOM Medical Device Registration
TRULIFE Pressure Care is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603021009. The device is manufactured by TRULIFE. from Ireland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ENDO INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
TRULIFE.Country of Origin
Ireland
Authorized Representative
PT. ENDO INDONESIAAR Address
Jl. Raya Menganti 14
Registration Date
Jun 03, 2024
Expiry Date
Mar 21, 2027
Product Type
Surgical Equipment
Operating tables and accessories and operating chairs and accessories.
Non Electromedic Non Sterile
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