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ADSS Electromagnetic Stimulator Device - Indonesia BPOM Medical Device Registration

ADSS Electromagnetic Stimulator Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403420088. The device is manufactured by BEIJING ADSS DEVELOPMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. WIE JAYA 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 : B
ADSS Electromagnetic Stimulator Device
Analysis ID: AKL 21403420088

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. WIE JAYA INDONESIA

AR Address

JALAN BATU TULIS GANG ANDONG NOMOR 14 A, Desa/Kelurahan. Batu Tulis, Kec. Bogor Selatan, Kota Bogor, Provinsi Jawa Barat, Kode Pos: 16131

Registration Date

Mar 05, 2024

Expiry Date

Jan 01, 2028

Product Type

Therapeutic Physical Health Equipment

Powered muscle stimulator.

Non Radiation Electromedics

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