Pure Global

FENTEX FESS (FUNCTIONAL ENDOSCOPY SINUS SURGERY) Instrument Set - Indonesia BPOM Medical Device Registration

FENTEX FESS (FUNCTIONAL ENDOSCOPY SINUS SURGERY) Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703411436. The device is manufactured by FENTEXMEDICAL GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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 : A
FENTEX FESS (FUNCTIONAL ENDOSCOPY SINUS SURGERY) Instrument Set
Analysis ID: AKL 10703411436

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Mar 08, 2019

Expiry Date

Feb 04, 2024

Product Type

Ear, Nose and Throat Surgical Equipment

Ear, nose, and throat manual surgical instrument.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from FENTEXMEDICAL GMBH.
Products from the same manufacturer (1 products)