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MIACARE DELiGHT 1-Day Silicone Hydrogel Soft Contact Lens - Indonesia BPOM Medical Device Registration

MIACARE DELiGHT 1-Day Silicone Hydrogel Soft Contact Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204027441. The device is manufactured by VISCO TECHNOLOGY SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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
MIACARE DELiGHT 1-Day Silicone Hydrogel Soft Contact Lens
Analysis ID: AKL 21204027441

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Feb 11, 2025

Expiry Date

Nov 20, 2029

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens.

Non Electromedic Sterile

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