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EUNSUNG MESOMATE Infusion Device - Indonesia BPOM Medical Device Registration

EUNSUNG MESOMATE Infusion Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403111403. The device is manufactured by EUNSUNG GLOBAL CORP. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HERCA CIPTA DERMAL PERDANA.

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
EUNSUNG MESOMATE Infusion Device
Analysis ID: AKL 21403111403

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

HERCA CIPTA DERMAL PERDANA

AR Address

Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460

Registration Date

May 19, 2020

Expiry Date

Nov 11, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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