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DUK-IN Lite S - Indonesia BPOM Medical Device Registration

DUK-IN Lite S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11403220054. The device is manufactured by DUK-IN CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ENDO INDONESIA.

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 : A
DUK-IN Lite S
Analysis ID: AKL 11403220054

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

DUK-IN CO., LTD.

Country of Origin

Korea

Authorized Representative

ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Sep 26, 2023

Expiry Date

Sep 08, 2028

Product Type

Therapeutic Physical Health Equipment

Prosthetic and orthotic accessory.

Non Electromedic Non Sterile

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