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PROTECTALON 2.0% - Indonesia BPOM Medical Device Registration

PROTECTALON 2.0% is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203320363. The device is manufactured by VSY BIOTECHNOLOGY AND PHARMACEUTICAL INDUSTRY JOINT STOCK COMPANY from Turkey, and is classified as Risk Class Kelas Resiko : D. 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 : D
PROTECTALON 2.0%
Analysis ID: AKL 31203320363

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Turkey

Authorized Representative

PT. TRANSMEDIC INDONESIA

AR Address

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

Registration Date

Aug 18, 2023

Expiry Date

Jun 06, 2027

Product Type

Surgical Eye Equipment

Intraocular fluid.

Non Electromedic Sterile

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