Pure Global

FRESCO Heparin Cap - Indonesia BPOM Medical Device Registration

FRESCO Heparin Cap is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902126197. The device is manufactured by DISPOSAFE HEALTH AND LIFE CARE LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ABADINUSA USAHASEMESTA.

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 : C
FRESCO Heparin Cap
Analysis ID: AKL 20902126197

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. ABADINUSA USAHASEMESTA

AR Address

Jalan Raden Saleh No. 45 G

Registration Date

Oct 21, 2021

Expiry Date

Oct 19, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing