Pure Global

ACCU-CHEK FastClix Lancing Device - Indonesia BPOM Medical Device Registration

ACCU-CHEK FastClix Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603716427. The device is manufactured by BALDA MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ROCHE INDONESIA.

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
ACCU-CHEK FastClix Lancing Device
Analysis ID: AKL 11603716427

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

BALDA MEDICAL GMBH

Country of Origin

Germany

Authorized Representative

PT. ROCHE INDONESIA

AR Address

Gedung AIA Central Lantai 36 Jl. Jend. Sudirman KAV. 48A RT/RW 003/004 Kelurahan Karet Semanggi

Registration Date

Feb 20, 2023

Expiry Date

Sep 23, 2026

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing