Pure Global

E-LIFE LUMBARFIT Brace - Indonesia BPOM Medical Device Registration

E-LIFE LUMBARFIT Brace is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402025978. The device is manufactured by ZHANG PU ORTHOLIFE REHABILITATION CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SAPTA MANDIRI 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
E-LIFE LUMBARFIT Brace
Analysis ID: AKL 11402025978

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SAPTA MANDIRI INDONESIA

AR Address

jalan raya kalibata no.15

Registration Date

Oct 09, 2020

Expiry Date

Nov 19, 2024

Product Type

Prosthetic Physical Health Equipment

Limb orthosis.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing