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SEGES Meniscal Repair System - Indonesia BPOM Medical Device Registration

SEGES Meniscal Repair System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421223. The device is manufactured by HITIT-MED MEDICAL PRODUCTS CO. LTD. from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is WIJAYA MITRA HUSADA.

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 : C
SEGES Meniscal Repair System
Analysis ID: AKL 21603421223

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

WIJAYA MITRA HUSADA

AR Address

Jln. Sirojul Munir, Kp Cakung, Perum Pualam Green Village, Kav 2, RT 004/03, Jatisari, Jati Asih, Kota Bekasi

Registration Date

Jun 09, 2024

Expiry Date

Dec 31, 2026

Product Type

Surgical Equipment

Nonabsorbable poly(ethylene terephthalate) surgical suture.

Non Electromedic Sterile

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