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ZEISS Semi-Finished Freeform Puck 1.67 BlueGuard - Indonesia BPOM Medical Device Registration

ZEISS Semi-Finished Freeform Puck 1.67 BlueGuard is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204220158. The device is manufactured by CARL ZEISS VISION (CHINA) LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. VARIOUS ETERNAL GIFTS.

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 : A
ZEISS Semi-Finished Freeform Puck 1.67 BlueGuard
Analysis ID: AKL 11204220158

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. VARIOUS ETERNAL GIFTS

AR Address

Ruko Taman Galaxy, Jl. Nusa Indah Raya Blok W No.1A Kel. Jakasetia, Kec. Bekasi Selatan, Kota Bekasi, Jawa Barat

Registration Date

Jun 21, 2022

Expiry Date

Sep 30, 2025

Product Type

Therapeutic Eye Equipment

Prescription show lens.

Non Electromedic Non Sterile

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