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JEIL MEDICAL Surgical Instrument - Indonesia BPOM Medical Device Registration

JEIL MEDICAL Surgical Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603220444. The device is manufactured by JEIL MEDICAL CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FIXIPRIMA PERSADA.

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
JEIL MEDICAL Surgical Instrument
Analysis ID: AKL 10603220444

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

FIXIPRIMA PERSADA

AR Address

Jl. Pintu Air Raya No. 7, Blok B-5 Jakarta

Registration Date

Jan 25, 2023

Expiry Date

Oct 14, 2025

Product Type

Surgical Dental Equipment

Dental hand instrument

Non Electromedic Non Sterile

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