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TARGET Endoscopic Instrument - Indonesia BPOM Medical Device Registration

TARGET Endoscopic Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420280. The device is manufactured by SOLENDOS INC. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KIMERA FLUX 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
TARGET Endoscopic Instrument
Analysis ID: AKL 11303420280

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

SOLENDOS INC.

Country of Origin

Korea

Authorized Representative

PT. KIMERA FLUX INDONESIA

AR Address

Ruko Melati Vista V21/A2 Jl.Boulevard

Registration Date

Aug 26, 2024

Expiry Date

Jul 09, 2026

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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