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PERISPONGE Absorbable Gelatine Sponge - Indonesia BPOM Medical Device Registration

PERISPONGE Absorbable Gelatine Sponge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31603220933. The device is manufactured by AEGIS LIFESCIENCES PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. DENTAL JAYA INDONESIA.

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
PERISPONGE Absorbable Gelatine Sponge
Analysis ID: AKL 31603220933

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

PT. DENTAL JAYA INDONESIA

AR Address

Jalan A.M.Sangaji Nomor 71A

Registration Date

Apr 13, 2022

Expiry Date

Jun 17, 2026

Product Type

Surgical Equipment

Absorbable hemostatic agent and dressing.

Non Electromedic Sterile

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