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KINETIK WELLBEING Lancing Device - Indonesia BPOM Medical Device Registration

KINETIK WELLBEING Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603422940. The device is manufactured by BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KIMIA FARMA TRADING & DISTRIBUTION.

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
KINETIK WELLBEING Lancing Device
Analysis ID: AKL 11603422940

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

AR Address

JL.BUDI UTOMO NO.1

Registration Date

Dec 22, 2024

Expiry Date

Jan 31, 2029

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Non Sterile

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