Pure Global

CeraSeal - Indonesia BPOM Medical Device Registration

CeraSeal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602320634. The device is manufactured by META BIOMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REVO MEDIKA PARAHYANGAN.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
CeraSeal
Analysis ID: AKL 20602320634

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. REVO MEDIKA PARAHYANGAN

AR Address

Jl. Batununggal Indah II Ruko Blok RD 17 RT.01/RW.05, Desa/Kelurahan Mengger, Kec. Bandung Kidul, Kota Bandung, Provinsi Jawa Barat, Kode Pos: 40267

Registration Date

Aug 01, 2023

Expiry Date

Mar 22, 2027

Product Type

Prosthetic Dental Equipment

Root canal filling resin

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing