MEDICOP Direct Vacuum Regulator with Safety Jar - Indonesia BPOM Medical Device Registration
MEDICOP Direct Vacuum Regulator with Safety Jar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903221280. The device is manufactured by MEDICOP D.O.O from Slovenia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SEKAR SURYA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDICOP D.O.OCountry of Origin
Slovenia
Authorized Representative
SEKAR SURYA MANDIRIAR Address
The ICON Business Park, Blok J No. 5 BSD City Tangerang, Banten
Registration Date
Nov 16, 2022
Expiry Date
May 18, 2026
Product Type
General Hospital Equipment and Other Individuals
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