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K-RECLAR Galvanic Water Peeler - Indonesia BPOM Medical Device Registration

K-RECLAR Galvanic Water Peeler is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003320121. The device is manufactured by RNU CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MERDIS INTERNATIONAL.

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
K-RECLAR Galvanic Water Peeler
Analysis ID: AKL 21003320121

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

RNU CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. MERDIS INTERNATIONAL

AR Address

Gedung DBS Bank Tower Lt.12, Unit 1202 A. Ciputra World 1 Jl. Prof. Dr. Satrio Kav.3-5, Karet Kuningan, Setiabudi, Jakarta Selatan

Registration Date

May 08, 2023

Expiry Date

Feb 10, 2028

Product Type

Therapeutic Neurology Equipment

Transcutaneous electrical nerve stimulator for pain relief.

Non Radiation Electromedics

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