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SURGITRON Dual 120 and All Accessories - Indonesia BPOM Medical Device Registration

SURGITRON Dual 120 and All Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603912394. The device is manufactured by CYNOSURE, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is CITRA VITA BUANA.

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BPOM Registered
Risk Class Kelas Resiko : C
SURGITRON Dual 120 and All Accessories
Analysis ID: AKL 21603912394

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

CYNOSURE, INC.

Country of Origin

United States

Authorized Representative

CITRA VITA BUANA

AR Address

Jalan M Hasibuan Ruko Suncity Square Bkok E-18 RT 004 RW 002

Registration Date

Nov 22, 2023

Expiry Date

Dec 31, 2025

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Radiation Electromedics

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