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REDURA (Regenerative Dural Repair Patch) - Indonesia BPOM Medical Device Registration

REDURA (Regenerative Dural Repair Patch) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003712539. The device is manufactured by MEDPRIN REGENERATIVE MEDICAL TECHNOLOGIES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BRIDGE TWO.

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
REDURA (Regenerative Dural Repair Patch)
Analysis ID: AKL 21003712539

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Aug 21, 2023

Expiry Date

Oct 30, 2025

Product Type

Therapeutic Neurology Equipment

Dura substitute.

Non Electromedic Sterile

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