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MSD Meniscus Trial Lenses Set - Indonesia BPOM Medical Device Registration

MSD Meniscus Trial Lenses Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201320446. The device is manufactured by FE-GROUP SRL COMPANY from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TRIASTRI MEDITAMA.

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
MSD Meniscus Trial Lenses Set
Analysis ID: AKL 11201320446

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Italy

Authorized Representative

TRIASTRI MEDITAMA

AR Address

JL. INDUSTRI NO.9-11 GUNUNG SAHARI UTARA,

Registration Date

Dec 27, 2023

Expiry Date

Jan 27, 2028

Product Type

Diagnostic Eye Equipment

Ophthalmic trial lens set.

Non Electromedic Non Sterile

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