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ALARIS PK Plus Syringe Pump - Indonesia BPOM Medical Device Registration

ALARIS PK Plus Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902918936. The device is manufactured by PLEXUS RO S.R.L. from Romania, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BECTON DICKINSON INDONESIA.

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
ALARIS PK Plus Syringe Pump
Analysis ID: AKL 20902918936

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PLEXUS RO S.R.L.

Country of Origin

Romania

Authorized Representative

PT. BECTON DICKINSON INDONESIA

AR Address

Sampoerna Strategic Square South Tower 20th Floor, Jl. Jenderal Sudirman Kav. 45-46

Registration Date

Feb 13, 2023

Expiry Date

Aug 22, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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