Pure Global

LILMOON Contact Lens For All Day Activities - Indonesia BPOM Medical Device Registration

LILMOON Contact Lens For All Day Activities is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204420289. The device is manufactured by FUJIAN UNICON OPTICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. LILA SEHAT MEDICAL TECHNOLOGY.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
LILMOON Contact Lens For All Day Activities
Analysis ID: AKL 21204420289

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. LILA SEHAT MEDICAL TECHNOLOGY

AR Address

Bukti Golf Mediterania Rukan Ekslusif, Jl. Marina Raya Blok C No. 30, Desa/Kelurahan Kamal Muara, Kec. Penjaringan, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta Utara Kode Pos : 14470

Registration Date

Jul 02, 2024

Expiry Date

Jul 01, 2027

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing