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ASKINA Calgitrol AG - Indonesia BPOM Medical Device Registration

ASKINA Calgitrol AG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603212894. The device is manufactured by B. BRAUN HOSPICARE LIMITED from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. B. BRAUN MEDICAL 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 : B
ASKINA Calgitrol AG
Analysis ID: AKL 21603212894

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Ireland

Authorized Representative

PT. B. BRAUN MEDICAL INDONESIA

AR Address

Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan

Registration Date

Dec 15, 2020

Expiry Date

Oct 04, 2024

Product Type

Surgical Equipment

Hydrophilic wound dressing

Non Electromedic Sterile

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