PLASON Air-Plasma Scalpel-Coagulator-Stimulator - Indonesia BPOM Medical Device Registration
PLASON Air-Plasma Scalpel-Coagulator-Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603124613. The device is manufactured by CENTER BAUMAN MOSCOW STATE TECHNICAL UNIVERSITY (CENTER BMSTU), LLC from Russia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FIRST MEDIKACITRA CENTER.
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
Country of Origin
Russia
Authorized Representative
PT. FIRST MEDIKACITRA CENTERAR Address
Jl. Paseban Raya No. 21 Salemba
Registration Date
Jul 29, 2021
Expiry Date
Feb 01, 2024
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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