Pure Global

FORA Lancing Device - Indonesia BPOM Medical Device Registration

FORA Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603912702. The device is manufactured by TAIDOC TECHNOLOGY CORPORATION. from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INNOVATION HEALTHCARE 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
FORA Lancing Device
Analysis ID: AKL 11603912702

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Taiwan (China)

Authorized Representative

PT. INNOVATION HEALTHCARE INDONESIA

AR Address

Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450

Registration Date

Dec 31, 2022

Expiry Date

Apr 01, 2027

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing