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JEIL Surgical Instrument - Indonesia BPOM Medical Device Registration

JEIL Surgical Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303916621. 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 PT. FAJAR SELARAS PARTNERS.

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 Surgical Instrument
Analysis ID: AKL 11303916621

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

PT. FAJAR SELARAS PARTNERS

AR Address

RUKAN PULOGADUNG TRADE CENTRE (PTC) BLOK 8C NOMOR 28-29

Registration Date

Aug 13, 2024

Expiry Date

Jul 04, 2029

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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