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CANACK Vivi Cup - Indonesia BPOM Medical Device Registration

CANACK Vivi Cup is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104320618. The device is manufactured by NINGBO LUKE MEDICAL DEVICES CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GENKI SEHAT 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
CANACK Vivi Cup
Analysis ID: AKL 21104320618

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GENKI SEHAT INDONESIA

AR Address

Jalan KH WAHID HASYIM NO 62A

Registration Date

Oct 14, 2023

Expiry Date

Jun 26, 2028

Product Type

Therapeutic Obstetric and Gynecological Equipment

Menstrual cup.

Non Electromedic Non Sterile

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