Pure Global

BIOGLUE® Surgical Adhesive - Indonesia BPOM Medical Device Registration

BIOGLUE® Surgical Adhesive is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31603324628. The device is manufactured by ARTIVION, INC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is GLOBAL DISPOMEDIKA.

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 : D
BIOGLUE® Surgical Adhesive
Analysis ID: AKL 31603324628

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

ARTIVION, INC.

Country of Origin

United States

Authorized Representative

GLOBAL DISPOMEDIKA

AR Address

Jl. Penjernihan 1 No. 38 Lt. 2

Registration Date

Aug 12, 2023

Expiry Date

Mar 20, 2028

Product Type

Surgical Equipment

Tissue adhesive for non-topical use

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing