Pure Global

PERMAMEM - Indonesia BPOM Medical Device Registration

PERMAMEM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220357. The device is manufactured by MEBIOS 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
PERMAMEM
Analysis ID: AKL 20602220357

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEBIOS GMBH

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

Nov 21, 2022

Expiry Date

Feb 09, 2027

Product Type

Prosthetic Dental Equipment

Polytetrafluoroethylene (PTFE) vitreous carbon materials.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from MEBIOS GMBH
Products from the same manufacturer (1 products)