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.
Risk Classification
Product Class
Kelas : 3
Manufacturer
AEGIS LIFESCIENCES PVT. LTD.Country of Origin
India
Authorized Representative
PT. DENTAL JAYA INDONESIAAR 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.
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