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RTA i LED II - Indonesia BPOM Medical Device Registration

RTA i LED II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605420488. The device is manufactured by GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRI ANUGERAH JAYA.

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 : B
RTA i LED II
Analysis ID: AKL 20605420488

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TRI ANUGERAH JAYA

AR Address

Jl. Raya Pos Pengumben 34 G

Registration Date

Dec 19, 2024

Expiry Date

Jul 17, 2029

Product Type

Other Dental Equipment

Ultraviolet activator for polymerization.

Non Radiation Electromedics

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