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KEYOUNG Dental Air Compressor - Indonesia BPOM Medical Device Registration

KEYOUNG Dental Air Compressor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605420467. The device is manufactured by FOSHAN KEYOUNG MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. THOMASONG NIRMALA.

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
KEYOUNG Dental Air Compressor
Analysis ID: AKL 10605420467

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. THOMASONG NIRMALA

AR Address

Jl. AM. Sangaji No. 20A

Registration Date

Nov 18, 2024

Expiry Date

Aug 01, 2029

Product Type

Other Dental Equipment

Dental operative unit and accessories.

Non Radiation Electromedics

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