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BERDIA UV Phototherapy - Indonesia BPOM Medical Device Registration

BERDIA UV Phototherapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420792. The device is manufactured by KERNEL MEDICAL EQUIPMENT CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GROW IN LINE WITH FORCE.

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
BERDIA UV Phototherapy
Analysis ID: AKL 21603420792

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GROW IN LINE WITH FORCE

AR Address

City Square Bussiness Park Blok B No. 66 Jl. Peta Selatan RT 10/01 Kalideres Jakarta

Registration Date

Apr 05, 2024

Expiry Date

Apr 05, 2027

Product Type

Surgical Equipment

Ultraviolet lamp for dermatologic disorders.

Non Radiation Electromedics

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