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PRECISION 1 ™ - Indonesia BPOM Medical Device Registration

PRECISION 1 ™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204126616. The device is manufactured by CIBA VISION ASIAN MANUFACTURING AND LOGISTICS PTE LTD. from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRACE ARGON MEDICA.

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
PRECISION 1 ™
Analysis ID: AKL 21204126616

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Singapore

Authorized Representative

PT. GRACE ARGON MEDICA

AR Address

Titan Center Lantai 4, Jl. Boulevard Bintaro Blok B7/B1 No. 5 Bintaro Jaya Sektor 7

Registration Date

Aug 01, 2024

Expiry Date

Mar 31, 2027

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens.

Non Electromedic Sterile

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