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TI-OSS Syringe - Indonesia BPOM Medical Device Registration

TI-OSS Syringe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220003. The device is manufactured by CHIYEWON CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ISCO LOGISTICS 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 : C
TI-OSS Syringe
Analysis ID: AKL 20602220003

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

CHIYEWON CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. ISCO LOGISTICS INDONESIA

AR Address

JL. H.R. MOCH. MANGUNDIPROJO NO. 1A

Registration Date

Jan 18, 2022

Expiry Date

Aug 25, 2026

Product Type

Prosthetic Dental Equipment

Bone grafting material.

Non Electromedic Sterile

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