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TECHNO MEDICA Flush Solution - Indonesia BPOM Medical Device Registration

TECHNO MEDICA Flush Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204719168. The device is manufactured by TECHNO MEDICA CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GANDASARI EKASATYA.

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
TECHNO MEDICA Flush Solution
Analysis ID: AKL 10204719168

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

PT. GANDASARI EKASATYA

AR Address

Jl. Raya HANKAM No.9A RT.007/002 Kel. Bambu Apus, Kec. Cipayung 13890

Registration Date

Aug 01, 2024

Expiry Date

Dec 31, 2026

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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