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LIGAFLEX POST-OP - Indonesia BPOM Medical Device Registration

LIGAFLEX POST-OP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11403610704. The device is manufactured by THUASNE. from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BETWEEN PARTNERS OF SELF-SUFFICIENCY.

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
LIGAFLEX POST-OP
Analysis ID: AKL 11403610704

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

THUASNE.

Country of Origin

France

Authorized Representative

PT. BETWEEN PARTNERS OF SELF-SUFFICIENCY

AR Address

Jl. Pos Pengumben Raya No.8 RT.005 RW.005, Sukabumi Selatan, Kebon Jeruk, Jakarta Barat 11560

Registration Date

Jun 06, 2020

Expiry Date

Jan 08, 2025

Product Type

Therapeutic Physical Health Equipment

Prosthetic and orthotic accessory.

Non Electromedic Non Sterile

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PRODEVICE Combo Pack Kateterisasi Urin A

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Kelas Resiko : A

PRODEVICE Combo Pack Pen

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Kelas Resiko : C

PRODEVICE Combo Pack Kateterisasi Urin B

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Kelas Resiko : C

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Kelas Resiko : A

PD Fix

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VENOFLEX Kokoon Absolu Stocking C2

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Kelas Resiko : A

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