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MEDAX - Biopsy Needle mod. MIELOX - Indonesia BPOM Medical Device Registration

MEDAX - Biopsy Needle mod. MIELOX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10801220154. The device is manufactured by MEDAX S.R.L UNIPERSONALE from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BIOZATIX INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
MEDAX - Biopsy Needle mod. MIELOX
Analysis ID: AKL 10801220154

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Italy

Authorized Representative

PT. BIOZATIX INDONESIA

AR Address

Green Sedayu Bizpark Cakung Blok GS 9A No. 12, Jl. Cakung Cilincing Raya KM. 02 RT.11/RW.06, Kode Pos 13910

Registration Date

Nov 12, 2024

Expiry Date

Dec 07, 2028

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument (biopsy forceps cover and non-electric biopsy forceps)

Non Electromedic Sterile

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