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ABN Aspira Suction Unit - Indonesia BPOM Medical Device Registration

ABN Aspira Suction Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603323168. The device is manufactured by EMG TECHNOLOGY CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ABADINUSA USAHASEMESTA.

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
ABN Aspira Suction Unit
Analysis ID: AKL 21603323168

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. ABADINUSA USAHASEMESTA

AR Address

Jalan Raden Saleh No. 45 G

Registration Date

Feb 01, 2023

Expiry Date

Jan 25, 2026

Product Type

Surgical Equipment

Powered suction pump.

Non Radiation Electromedics

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