Pure Global

HEMOLOK Gel - Indonesia BPOM Medical Device Registration

HEMOLOK Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603716847. The device is manufactured by THEMIS MEDICARE LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.

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
HEMOLOK Gel
Analysis ID: AKL 21603716847

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. BRIDGE TWO

AR Address

Petojo Melintang No. 17 Kel. Petojo Selatan, Kec. Gambir Jakarta Pusat

Registration Date

Dec 29, 2020

Expiry Date

Sep 22, 2025

Product Type

Surgical Equipment

Hydrophilic wound dressing

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing