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PIGEON Manual Breast Pump - Indonesia BPOM Medical Device Registration

PIGEON Manual Breast Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11104320512. The device is manufactured by PIGEON INDUSTRIES (THAILAND) CO.,LTD from Thailand, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MULTI INDOCITRA.

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
PIGEON Manual Breast Pump
Analysis ID: AKL 11104320512

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Thailand

Authorized Representative

PT. MULTI INDOCITRA

AR Address

Green Central City, Commercial Area Lantai 6, Jl. Gajah Mada No.188, RT.3/RW.5, Glodok, Taman Sari, Jakarta Barat 11120

Registration Date

Jul 25, 2023

Expiry Date

Sep 20, 2026

Product Type

Therapeutic Obstetric and Gynecological Equipment

Nonpowered breast pump.

Non Electromedic Non Sterile

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