Pure Global

GLOPACK Plasma Indicator Tape - Indonesia BPOM Medical Device Registration

GLOPACK Plasma Indicator Tape is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20901320549. The device is manufactured by ANQING KANGMINGNA PACKAGING CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOMED ADINATA PRIMA.

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
GLOPACK Plasma Indicator Tape
Analysis ID: AKL 20901320549

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GLOMED ADINATA PRIMA

AR Address

Jl. Gunung Sahari Raya No.2 Blok E/23-A Kelurahan : Pademangan Barat Kecamatan : Pademangan

Registration Date

Jul 24, 2023

Expiry Date

Feb 08, 2026

Product Type

General and Individual Hospital Equipment Monitoring

Sterilization process indicator.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing