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A Vitan Inserter folder - Indonesia BPOM Medical Device Registration

A Vitan Inserter folder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203123122. The device is manufactured by DUCKWORTH & KENT, LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BRIDGE TWO.

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 : A
A Vitan Inserter folder

UNFOLDER Vitan Inserter

Analysis ID: AKL 21203123122

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United Kingdom

Authorized Representative

PT. BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Dec 12, 2024

Expiry Date

Aug 19, 2027

Product Type

Surgical Eye Equipment

Intraocular lens guide

Non Electromedic Non Sterile

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