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PASTRA Acrylic Foldable Intraocular Lens - Indonesia BPOM Medical Device Registration

PASTRA Acrylic Foldable Intraocular Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202126876. The device is manufactured by EXCELLENT HI CARE PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ATHENS YOUNG 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 : D
PASTRA Acrylic Foldable Intraocular Lens
Analysis ID: AKL 31202126876

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

PT. ATHENS YOUNG INDONESIA

AR Address

AGUNG PODOMORO LAND TOWER - CENTRAL PARK LANTAI 17 UNIT T 1 (SUITE 1706) PODOMORO CITY JL LETJEND S.PARMAN KAV 28

Registration Date

Nov 15, 2021

Expiry Date

May 26, 2026

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

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