Pure Global

TEKNOMAR Hydrogen Peroxide Plasma Sterilization Device S125 Single Door - Indonesia BPOM Medical Device Registration

TEKNOMAR Hydrogen Peroxide Plasma Sterilization Device S125 Single Door is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903220161. The device is manufactured by TEKNOMAR MAKINA IMALAT ITH. IHR. SAN VE TIC. LTD.. STI from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is JEMA INDO MANDIRI.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
TEKNOMAR Hydrogen Peroxide Plasma Sterilization Device S125 Single Door
Analysis ID: AKL 20903220161

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

JEMA INDO MANDIRI

AR Address

Jl. RS. Fatmawati No. 100 E Cilandak Jakarta Selatan

Registration Date

Feb 10, 2022

Expiry Date

Sep 20, 2025

Product Type

General Hospital Equipment and Other Individuals

Plasma Sterilizer

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from TEKNOMAR MAKINA IMALAT ITH. IHR. SAN VE TIC. LTD.. STI
Products from the same manufacturer (1 products)