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LIGHTTRAIL Single Use Laser Fibers - Indonesia BPOM Medical Device Registration

LIGHTTRAIL Single Use Laser Fibers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603718833. The device is manufactured by BOSTON SCIENTIFIC LIMITED from Ireland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BOSTON SCIENTIFIC 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
LIGHTTRAIL Single Use Laser Fibers
Analysis ID: AKL 21603718833

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Ireland

Authorized Representative

PT. BOSTON SCIENTIFIC INDONESIA

AR Address

Prudential Tower lantai 28 Jl. Jend. Sudirman Kav. 79

Registration Date

Sep 21, 2022

Expiry Date

Apr 20, 2027

Product Type

Surgical Equipment

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

Non Electromedic Sterile

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