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HEMCON ChitoGauze XR PRO - Indonesia BPOM Medical Device Registration

HEMCON ChitoGauze XR PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603422030. The device is manufactured by TRICOL BIOMEDICAL, INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. RANAYA FAZZA UTAMA.

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
HEMCON ChitoGauze XR PRO
Analysis ID: AKL 11603422030

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. RANAYA FAZZA UTAMA

AR Address

Ruko Grand Wisata, Festive Garden Blok/KAV AA16/53

Registration Date

Aug 30, 2024

Expiry Date

Jan 14, 2027

Product Type

Surgical Equipment

Nonresorbable gauze/sponge for external use, non sterile

Non Electromedic Non Sterile

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