GUNA MD-Tissue H - Indonesia BPOM Medical Device Registration
GUNA MD-Tissue H is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302420464. The device is manufactured by USE S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is I-TECH LAFACOS.
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.
Risk Classification
Product Class
Kelas : 3
Manufacturer
USE S.P.A.Country of Origin
Italy
Authorized Representative
I-TECH LAFACOSAR Address
Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih
Registration Date
Nov 26, 2024
Expiry Date
May 31, 2027
Product Type
Prosthetic Orthopedic Equipment
Intra articular fluid
Non Electromedic Sterile

