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MEDIATECH Pompa Asi Manual - Indonesia BPOM Medical Device Registration

MEDIATECH Pompa Asi Manual is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11104124467. The device is manufactured by NINGBO REAL BUBEE MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDIA TECHNOLOGY.

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
MEDIATECH Pompa Asi Manual
Analysis ID: AKL 11104124467

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. MEDIA TECHNOLOGY

AR Address

KOMPLEK INKOPAL BLOK C NO.71 JL.BOULEVARD BARAT RAYA, KEL.KELAPA GADING

Registration Date

Jun 24, 2024

Expiry Date

Jun 24, 2027

Product Type

Therapeutic Obstetric and Gynecological Equipment

Nonpowered breast pump.

Non Electromedic Non Sterile

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