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SAESHIN E-CUBE Endomotor - Indonesia BPOM Medical Device Registration

SAESHIN E-CUBE Endomotor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603124499. The device is manufactured by SAESHIN PRECISION CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BINTANG SAUDARA SEMESTA JAYA.

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
SAESHIN E-CUBE Endomotor
Analysis ID: AKL 20603124499

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. BINTANG SAUDARA SEMESTA JAYA

AR Address

Jl.Asia No.212 A-B, Medan

Registration Date

Jun 24, 2021

Expiry Date

Mar 31, 2026

Product Type

Surgical Dental Equipment

Dental handpiece and accessories

Non Radiation Electromedics

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