RIESTER E-Scope Ophthalmoscope - Indonesia BPOM Medical Device Registration
RIESTER E-Scope Ophthalmoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201515531. The device is manufactured by RUDOLF RIESTER GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RUDOLF RIESTER GMBH.Country of Origin
Germany
Authorized Representative
PT. LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47
Registration Date
Jun 18, 2021
Expiry Date
Dec 31, 2025
Product Type
Diagnostic Eye Equipment
Ophthalmoscope.
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