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I-DROP MGD - Indonesia BPOM Medical Device Registration

I-DROP MGD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204321112. The device is manufactured by EXCELVISION from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRANSMEDIC 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
I-DROP MGD
Analysis ID: AKL 21204321112

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

EXCELVISION

Country of Origin

France

Authorized Representative

PT. TRANSMEDIC INDONESIA

AR Address

PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137

Registration Date

Nov 09, 2023

Expiry Date

Jan 31, 2028

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens care products.

Non Electromedic Sterile

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