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TECNIS 1-Piece IOL - Indonesia BPOM Medical Device Registration

TECNIS 1-Piece IOL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202124612. The device is manufactured by AMO PUERTO RICO MANUFACTURING, INC. from United States, and is classified as Risk Class Kelas Resiko : D. 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 : D
TECNIS 1-Piece IOL
Analysis ID: AKL 31202124612

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United States

Authorized Representative

PT. BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Dec 13, 2024

Expiry Date

Aug 19, 2027

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

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