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SUNRISE Syringe Pump - Indonesia BPOM Medical Device Registration

SUNRISE Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220540. The device is manufactured by SHENZHEN HAWK MEDICAL INSTRUMENT CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PETRA GRACIA CREATIONS.

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
SUNRISE Syringe Pump
Analysis ID: AKL 20902220540

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PETRA GRACIA CREATIONS

AR Address

Rukan Sedayu Square Blok J Mo.37 Rt.005 Rw.012 Jl. Lingkar Luar (Outer Ringroad) Cengkareng Kel. Cengkareng Barat Kec. Cengkareng Jakarta Ba

Registration Date

Jun 09, 2022

Expiry Date

Jun 08, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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