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SELEPUMP inflation device - Indonesia BPOM Medical Device Registration

SELEPUMP inflation device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320650. The device is manufactured by KOSSEL MEDTECH (SUZHOU) CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RIMATANDU MOTARO PRATAMA.

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
SELEPUMP inflation device
Analysis ID: AKL 20501320650

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. RIMATANDU MOTARO PRATAMA

AR Address

KANKO BLOK J7 NO.17PERUM METLAND MENTENG 011/007 KEL.UJUNG MENTENG,KEC.CAKUNG

Registration Date

Mar 29, 2023

Expiry Date

Sep 26, 2026

Product Type

Diagnostic Cardiology Equipment

Angiographic injector and syringe.

Non Electromedic Sterile

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