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MD-ChelCream - Indonesia BPOM Medical Device Registration

MD-ChelCream is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10602320665. The device is manufactured by META BIOMED CO., LTD., from Korea, and is classified as Risk Class Kelas Resiko : A. 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.

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BPOM Registered
Risk Class Kelas Resiko : A
MD-ChelCream
Analysis ID: AKL 10602320665

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

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 14, 2023

Expiry Date

Mar 22, 2027

Product Type

Prosthetic Dental Equipment

Root canal post.

Non Electromedic Non Sterile

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