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LKTECH ENDOLASER - Indonesia BPOM Medical Device Registration

LKTECH ENDOLASER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420548. The device is manufactured by TRIANGEL RSD LIMITED CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. JAMBERDETAK DERMA TECH.

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
LKTECH ENDOLASER
Analysis ID: AKL 21603420548

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. JAMBERDETAK DERMA TECH

AR Address

KOMPLEK PAKUAN, Jl. INTAN PAKUAN II NOMOR 2, RT 002 RW 007

Registration Date

Mar 05, 2024

Expiry Date

Mar 05, 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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