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MEDTRONIC Sil Serter - Indonesia BPOM Medical Device Registration

MEDTRONIC Sil Serter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903512836. The device is manufactured by SMC COSTA RICA DIVISION S.R.L. from Costa Rica, and is classified as Risk Class Kelas Resiko : B. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
MEDTRONIC Sil Serter
Analysis ID: AKL 20903512836

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Costa Rica

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Mar 06, 2020

Expiry Date

Apr 10, 2024

Product Type

General Hospital Equipment and Other Individuals

Syringe needle introducer.

Non Electromedic Non Sterile

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