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PEKFUTECH Infusion Pump - Indonesia BPOM Medical Device Registration

PEKFUTECH Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420817. The device is manufactured by MEDEVO MEDICAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PROCARE MEDITECH LIGHT.

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
PEKFUTECH Infusion Pump
Analysis ID: AKL 20902420817

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PROCARE MEDITECH LIGHT

AR Address

Jl. Jakarta Garden City, Ruko New East Blok. NE, No.39

Registration Date

Aug 07, 2024

Expiry Date

Jun 30, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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