PROMESH SURG DOME - Indonesia BPOM Medical Device Registration
PROMESH SURG DOME is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602024797. The device is manufactured by COUSIN BIOTECH S.A.S from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL DISPOMEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
COUSIN BIOTECH S.A.SCountry of Origin
France
Authorized Representative
PT. GLOBAL DISPOMEDIKAAR Address
Jl. Penjernihan 1 No. 38 Lt. 2
Registration Date
Sep 26, 2022
Expiry Date
Dec 31, 2024
Product Type
Prosthetic Surgical Equipment
Surgical mesh.
Non Electromedic Sterile
PROMESH SURG ABSO
PROMESH SURG UMB SR
PROMESH SURG ST
PROMESH SURG ABSO ANAT
PROMESH SURG LI
PROMESH SURG FLEXIL
PROMESH SURG UMB
PROMESH ยฎ ARISES ABSO VENT
PROMESH SURG INTRA
MONOTIME
PETERS SURGICAL
ACIER Stainless Steel Suture
PETERS SURGICAL
EIGHTH
PETERS SURGICAL
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