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ALLGENS SkuHeal™ Bone Graft Material - Indonesia BPOM Medical Device Registration

ALLGENS SkuHeal™ Bone Graft Material is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602520051. The device is manufactured by ALLGENS MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PURE SOUTHEAST ASIA 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 : C
ALLGENS SkuHeal™ Bone Graft Material
Analysis ID: AKL 20602520051

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PURE SOUTHEAST ASIA INDONESIA

AR Address

Equity Tower, 26th Floor H, Kav 52-53, Jl. Jenderal Sudirman

Registration Date

Feb 11, 2025

Expiry Date

Sep 23, 2029

Product Type

Prosthetic Dental Equipment

Bone grafting material.

Non Electromedic Sterile

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