PROFIMED Non Absorbable Suture - Indonesia BPOM Medical Device Registration
PROFIMED Non Absorbable Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603916988. The device is manufactured by MEDIPAC-TH KAZANTZIDIS S.A. from Greece, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ETERNAL GRACE.
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 : 2
Manufacturer
MEDIPAC-TH KAZANTZIDIS S.A.Country of Origin
Greece
Authorized Representative
PT. ETERNAL GRACEAR Address
JL Situ Aksan No 15 A RT 09, RW 10, Kel Sukahaji, Kec Babakan Ciparay
Registration Date
Oct 28, 2019
Expiry Date
May 15, 2024
Product Type
Surgical Equipment
Nonabsorbable expanded polytetrafluoroethylene surgical suture.
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