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PRO-TOUCH Vectra Diode laser system - Indonesia BPOM Medical Device Registration

PRO-TOUCH Vectra Diode laser system is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603918361. The device is manufactured by XINTEC CORPORATION DBA CONVERGENT LASER TECHNOLOGIES from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SIGMA KARSA MAGNA.

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
PRO-TOUCH Vectra Diode laser system
Analysis ID: AKL 21603918361

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

SIGMA KARSA MAGNA

AR Address

Ruko Mega Grosir Cempaka Mas, Jl. Letjen Suprapto Blok J No. 37-38 RW.08, Kel. Sumur Batu, Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta

Registration Date

Sep 07, 2023

Expiry Date

Sep 30, 2027

Product Type

Surgical Equipment

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

Non Radiation Electromedics

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