JENA MultiPulse HoPLUS - Indonesia BPOM Medical Device Registration
JENA MultiPulse HoPLUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603615251. The device is manufactured by JENA SURGICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRATIA JAYA MULYA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
JENA SURGICAL GMBHCountry of Origin
Germany
Authorized Representative
PT. GRATIA JAYA MULYAAR Address
Gading Park View, Jl. Boulevard Timur Raya Blok ZC I No. 10-11 Kelapa Gading
Registration Date
Dec 12, 2018
Expiry Date
Dec 03, 2023
Product Type
Surgical Equipment
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