SURTRON 120 - Indonesia BPOM Medical Device Registration
SURTRON 120 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603913258. The device is manufactured by LED S.p.A. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is CITRA PERSADA MEDICINDO.
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
LED S.p.A.Country of Origin
Italy
Authorized Representative
CITRA PERSADA MEDICINDOAR Address
Jl. DR. Ratulangi No. 7 B-1 Makassar Sulawesi Selatan
Registration Date
Nov 18, 2024
Expiry Date
Oct 29, 2029
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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