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GENTLE YAG Pro U - Indonesia BPOM Medical Device Registration

GENTLE YAG Pro U is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603122033. The device is manufactured by NPA DE MEXICO, S, DE, RL DE CV from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.

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.

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BPOM Registered
Risk Class Kelas Resiko : C
GENTLE YAG Pro U
Analysis ID: AKL 21603122033

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Sultan Iskandar Muda No. 7A & B

Registration Date

Apr 16, 2021

Expiry Date

May 01, 2025

Product Type

Surgical Equipment

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

Non Radiation Electromedics

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