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SCHWIND PERAMIS - Indonesia BPOM Medical Device Registration

SCHWIND PERAMIS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201121698. The device is manufactured by SCHWIND EYE-TECH-SOLUTIONS GMBH & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. 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
SCHWIND PERAMIS
Analysis ID: AKL 11201121698

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. TRIASTRI MEDITAMA

AR Address

GRIYA KEMAYORAN BLOK R-41 JL. INDUSTRI RAYA NO. 9-11

Registration Date

Feb 17, 2023

Expiry Date

May 01, 2027

Product Type

Diagnostic Eye Equipment

Keratoscope

Non Radiation Electromedics

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