Volumed®µVP7000 Chroma X - Indonesia BPOM Medical Device Registration
Volumed®µVP7000 Chroma X is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902221034. The device is manufactured by ARCOMED BY from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOSOPHA SAKTI.
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
ARCOMED BYCountry of Origin
Switzerland
Authorized Representative
PT. INDOSOPHA SAKTIAR Address
JL. MAMPANG PRAPATAN RAYA NO.1
Registration Date
Jul 08, 2024
Expiry Date
Feb 22, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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