HEINE DELTA 30 PRO - Indonesia BPOM Medical Device Registration
HEINE DELTA 30 PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903420223. The device is manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HEINE OPTOTECHNIK GMBH & CO. KG.Country of Origin
Germany
Authorized Representative
SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Mar 05, 2024
Expiry Date
Feb 28, 2025
Product Type
General Hospital Equipment and Other Individuals
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