Pure Global

KARL STORZ Intubation Fiber Scope - Indonesia BPOM Medical Device Registration

KARL STORZ Intubation Fiber Scope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101313291. The device is manufactured by KARL STORZ SE & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ADVANCE MEDICARE CORPORA.

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
KARL STORZ Intubation Fiber Scope
Analysis ID: AKL 21101313291

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. ADVANCE MEDICARE CORPORA

AR Address

KOMPLEK PERKANTORAN DUTA MERLIN BLOK B-26, BLOK D 8-10 JALAN GAJAH MADA 3-5

Registration Date

Oct 11, 2022

Expiry Date

Jan 21, 2026

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing