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CULKAT Soft Contact Lens (Zest) - Indonesia BPOM Medical Device Registration

CULKAT Soft Contact Lens (Zest) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204420292. The device is manufactured by GANSU CONSTAR TECHNOLOGY GROUP CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BBG TRADA INDONESIA.

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
CULKAT Soft Contact Lens (Zest)
Analysis ID: AKL 21204420292

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BBG TRADA INDONESIA

AR Address

Soho Capital Lt. 43 Unit 05 - 05A, Jl. Letjen. S. Parman Kav. 28, RT 003 RW 005

Registration Date

Sep 20, 2024

Expiry Date

Feb 15, 2028

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens.

Non Electromedic Sterile

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