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MEDELA THOPAZ Cardiothoracic Drainage - Indonesia BPOM Medical Device Registration

MEDELA THOPAZ Cardiothoracic Drainage is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903413313. 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 THOPAZ Cardiothoracic Drainage
Analysis ID: AKL 20903413313

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 15, 2023

Expiry Date

Jul 31, 2028

Product Type

General Hospital Equipment and Other Individuals

Vacuum-powered body fluid suction apparatus.

Non Radiation Electromedics

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