Pure Global

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
PROFIMED Non Absorbable Suture
Analysis ID: AKL 21603916988

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Greece

Authorized Representative

PT. ETERNAL GRACE

AR 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.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from MEDIPAC-TH KAZANTZIDIS S.A.
Products from the same manufacturer (2 products)