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AntamaxClin® Interleave Non Woven / Soft Crepe (Blue/Green) - Indonesia BPOM Medical Device Registration

AntamaxClin® Interleave Non Woven / Soft Crepe (Blue/Green) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903913736. The device is manufactured by ANTAMAX MANUFACTURING SDN BHD from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIO AXION HEALTHINDO.

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
AntamaxClin® Interleave Non Woven / Soft Crepe (Blue/Green)
Analysis ID: AKL 20903913736

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. BIO AXION HEALTHINDO

AR Address

Komplek Golden Plaza Blok G39 - G42 Jl. RS Fatmawati No. 15

Registration Date

Jul 16, 2020

Expiry Date

Jan 23, 2025

Product Type

General Hospital Equipment and Other Individuals

Sterilization wrap.

Non Electromedic Non Sterile

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