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ANSCARE ChitoClot Pad - Indonesia BPOM Medical Device Registration

ANSCARE ChitoClot Pad is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31603810393. The device is manufactured by BENQ MATERIALS CORPORATION from Taiwan (China), and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MAIN REVASS 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 : D
ANSCARE ChitoClot Pad
Analysis ID: AKL 31603810393

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Taiwan (China)

Authorized Representative

PT. MAIN REVASS MEDIKA

AR Address

Jl. Dewi Sartika No. 4B RT 004/007 Kel. Cililitan Kec. Kramat jati

Registration Date

Feb 09, 2022

Expiry Date

Dec 29, 2026

Product Type

Surgical Equipment

Absorbable hemostatic agent and dressing.

Non Electromedic Sterile

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