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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.

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BPOM Registered
Risk Class Kelas Resiko : D
GUNA MD-Tissue H
Analysis ID: AKL 31302420464

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

USE S.P.A.

Country of Origin

Italy

Authorized Representative

I-TECH LAFACOS

AR 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

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