GERMITEC Antigermix E1 - Indonesia BPOM Medical Device Registration
GERMITEC Antigermix E1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903912968. The device is manufactured by GERMITEC from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GERMITECCountry of Origin
France
Authorized Representative
PT. MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Mar 10, 2022
Expiry Date
Nov 27, 2026
Product Type
General Hospital Equipment and Other Individuals
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