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MEDELA Breast Pump - Indonesia BPOM Medical Device Registration

MEDELA Breast Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105602272. The device is manufactured by MEDELA AG. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CITRA VITA BUANA.

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
MEDELA Breast Pump
Analysis ID: AKL 21105602272

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDELA AG.

Country of Origin

Switzerland

Authorized Representative

PT. CITRA VITA BUANA

AR Address

Jl. M. Hasibuan, Ruko Suncity Square Blok E-18

Registration Date

Mar 14, 2019

Expiry Date

Mar 13, 2024

Product Type

Therapeutic Obstetric and Gynecological Equipment

Powered breast pump.

Non Radiation Electromedics

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