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SURESEAL SE160 Tube Sealer - Indonesia BPOM Medical Device Registration

SURESEAL SE160 Tube Sealer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209713150. The device is manufactured by CENTRON CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FRISMED HOSLAB 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 : A
SURESEAL SE160 Tube Sealer
Analysis ID: AKL 10209713150

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

PT. FRISMED HOSLAB INDONESIA

AR Address

Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321

Registration Date

Nov 13, 2023

Expiry Date

Dec 31, 2026

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Heat-sealing device.

Non Radiation Electromedics

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