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SEGES Lena PEEK Interference Screw - Indonesia BPOM Medical Device Registration

SEGES Lena PEEK Interference Screw is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420215. 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 Lena PEEK Interference Screw
Analysis ID: AKL 21302420215

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

Prosthetic Orthopedic Equipment

Smooth or threaded metallic bone fixation fastener.

Non Electromedic Sterile

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