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MEDELA Suction Pump - Indonesia BPOM Medical Device Registration

MEDELA Suction Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603602278. 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 Suction Pump
Analysis ID: AKL 21603602278

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDELA AG.

Country of Origin

Switzerland

Authorized Representative

PT. CITRA VITA BUANA

AR Address

Jalan M Hasibuan Ruko Suncity Square Bkok E-18 RT 004 RW 002

Registration Date

Dec 27, 2023

Expiry Date

Jul 31, 2028

Product Type

Surgical Equipment

Powered suction pump.

Non Radiation Electromedics

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