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FUKE Electric Patient Chair - Indonesia BPOM Medical Device Registration

FUKE Electric Patient Chair is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903220383. The device is manufactured by TONGLU FUKE MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TRIADI LINTAS PERSADA.

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
FUKE Electric Patient Chair
Analysis ID: AKL 10903220383

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

TRIADI LINTAS PERSADA

AR Address

Ruko Exclusive Raden Inten Jl. Raden Inten II No. 80 Kav. 5

Registration Date

Sep 18, 2023

Expiry Date

Aug 23, 2028

Product Type

General Hospital Equipment and Other Individuals

Medical chair and table.

Non Radiation Electromedics

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