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MEDELA Swing Maxi Flex Electric Breastpump - Indonesia BPOM Medical Device Registration

MEDELA Swing Maxi Flex Electric Breastpump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104915759. 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 Swing Maxi Flex Electric Breastpump
Analysis ID: AKL 21104915759

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

Sep 06, 2019

Expiry Date

Dec 03, 2023

Product Type

Therapeutic Obstetric and Gynecological Equipment

Powered breast pump.

Non Radiation Electromedics

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