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CIGARS Dermis Allograft - Indonesia BPOM Medical Device Registration

CIGARS Dermis Allograft is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602320840. The device is manufactured by RTI SURGICAL, INC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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
CIGARS Dermis Allograft

PUROS Dermis Allograft

Analysis ID: AKL 20602320840

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

RTI SURGICAL, INC

Country of Origin

United States

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5

Registration Date

Nov 30, 2023

Expiry Date

Jun 19, 2028

Product Type

Prosthetic Dental Equipment

Bone grafting material.

Non Electromedic Sterile

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