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ANGISPONGE - Indonesia BPOM Medical Device Registration

ANGISPONGE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31603023103. The device is manufactured by ANGEL LIFE SCIENCE from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is ALFA MEDICA BROTHERS.

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 : D
ANGISPONGE
Analysis ID: AKL 31603023103

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

ANGEL LIFE SCIENCE

Country of Origin

India

Authorized Representative

ALFA MEDICA BROTHERS

AR Address

Ruko Pondok Cabe Mutiara B/21, RT002/005 Kel. Pondok Cabe Udik, Kec. Pamulang Kota Tangerang Selatan

Registration Date

Jun 07, 2020

Expiry Date

Feb 06, 2025

Product Type

Surgical Equipment

Absorbable hemostatic agent and dressing.

Non Electromedic Sterile

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