Pure Global

COVIDIEN Plain Gut Absorbable Suture - Indonesia BPOM Medical Device Registration

COVIDIEN Plain Gut Absorbable Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603616142. The device is manufactured by COVIDIEN from Dominican, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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
COVIDIEN Plain Gut Absorbable Suture
Analysis ID: AKL 21603616142

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

COVIDIEN

Country of Origin

Dominican

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama

Registration Date

Feb 05, 2025

Expiry Date

Feb 20, 2029

Product Type

Surgical Equipment

Absorbable surgical gut suture.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing