CODAN Syringe Pump - Indonesia BPOM Medical Device Registration
CODAN Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902815312. The device is manufactured by CODAN ARGUS AG. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DEMKA 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
CODAN ARGUS AG.Country of Origin
Switzerland
Authorized Representative
DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Dec 27, 2022
Expiry Date
Jun 29, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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