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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.

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BPOM Registered
Risk Class Kelas Resiko : C
PLASON Air-Plasma Scalpel-Coagulator-Stimulator
Analysis ID: AKL 21603124613

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Russia

Authorized Representative

PT. FIRST MEDIKACITRA CENTER

AR 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.

Non Radiation Electromedics

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