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CERABONE - Indonesia BPOM Medical Device Registration

CERABONE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220216. The device is manufactured by BOTISS BIOMATERIALS GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRATIA JAYA MULYA.

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
CERABONE
Analysis ID: AKL 20602220216

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. GRATIA JAYA MULYA

AR Address

Gading Park View Blok ZC.I No. 10-11 Jl. Boulevard Timur Raya

Registration Date

Sep 15, 2022

Expiry Date

Feb 09, 2027

Product Type

Prosthetic Dental Equipment

Bone grafting material.

Non Electromedic Sterile

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