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YOTAVIS Hypromellose Ophthalmic Solution USP 2% w/v - Indonesia BPOM Medical Device Registration

YOTAVIS Hypromellose Ophthalmic Solution USP 2% w/v is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203220117. The device is manufactured by AUROLAB from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. YOTA MEDIKA 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
YOTAVIS Hypromellose Ophthalmic Solution USP 2% w/v
Analysis ID: AKL 31203220117

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

AUROLAB

Country of Origin

India

Authorized Representative

PT. YOTA MEDIKA INDONESIA

AR Address

Ruko PulogadungTrade Center Blok 8-A No. 3 Lantai 1&2, Jl. Raya Bekasi KM 21

Registration Date

Sep 30, 2022

Expiry Date

Jun 23, 2025

Product Type

Surgical Eye Equipment

Intraocular fluid.

Non Electromedic Sterile

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