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KES ND:YAG Laser Therapy System - Indonesia BPOM Medical Device Registration

KES ND:YAG Laser Therapy System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603718305. The device is manufactured by BEIJING KES BIOLOGY TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BCS PRIMA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
KES ND:YAG Laser Therapy System
Analysis ID: AKL 21603718305

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BCS PRIMA INDONESIA

AR Address

Jl. Pondok Kopi Raya Blok A No. 8 RT 009 RW 010

Registration Date

Aug 26, 2021

Expiry Date

Aug 09, 2026

Product Type

Surgical Equipment

Laser surgical instrument for use in general and plastic surgery and in dermatology.

Non Radiation Electromedics

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