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LENSX Laser - Indonesia BPOM Medical Device Registration

LENSX Laser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203113063. The device is manufactured by ALCON RESEARCH LLC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BINASUKSES CANTEEN.

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
LENSX Laser
Analysis ID: AKL 21203113063

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

BINASUKSES CANTEEN

AR Address

Jl. Pulo Kambing II No. 26 Kawasan Industri Pulogadung, Kel. Jatinegara, Kec. Cakung, Kota Adm. Jakarta Timur, Provinsi DKI Jakarta, Kode Pos 13930

Registration Date

Aug 01, 2024

Expiry Date

Mar 31, 2027

Product Type

Surgical Eye Equipment

Ophthalmic laser.

Non Radiation Electromedics

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