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BIEGLER Automatic Pressure Infusor - Indonesia BPOM Medical Device Registration

BIEGLER Automatic Pressure Infusor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902212169. The device is manufactured by BIEGLER MEDZEN ELEKTRONIK. from Austria, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INDOPRIMA BIONET.

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.

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BPOM Registered
Risk Class Kelas Resiko : A
BIEGLER Automatic Pressure Infusor
Analysis ID: AKL 10902212169

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Austria

Authorized Representative

PT. INDOPRIMA BIONET

AR Address

Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150

Registration Date

Oct 10, 2022

Expiry Date

Jun 27, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Pressure infusor for an I.V. bag.

Non Radiation Electromedics

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