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OSMOCEL SI SIlicone Hydroporous Foam - Indonesia BPOM Medical Device Registration

OSMOCEL SI SIlicone Hydroporous Foam is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603025188. The device is manufactured by SHANGHAI ISO MEDICAL PRODUCTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ALEXA MEDIKA.

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
OSMOCEL SI SIlicone Hydroporous Foam
Analysis ID: AKL 11603025188

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. ALEXA MEDIKA

AR Address

Jl. Brigjen Katamso, Komplek Istana Prima 1 Blok B No. 9-10, Kel. Sei Mati, Kec. Medan Maimun, Kota Medan, Prov. Sumatera Utara 20159

Registration Date

Aug 07, 2024

Expiry Date

Aug 23, 2028

Product Type

Surgical Equipment

Occlusive wound dressing.

Non Electromedic Sterile

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