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RUMEX Glaucoma Set - Indonesia BPOM Medical Device Registration

RUMEX Glaucoma Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203320254. The device is manufactured by RUMEX INSTRUMENTS LTD., from Russia, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PANCARAYA KRISNAMANDIRI.

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
RUMEX Glaucoma Set
Analysis ID: AKL 11203320254

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Russia

Authorized Representative

PT. PANCARAYA KRISNAMANDIRI

AR Address

KOMPLEK FATMAWATI MAS BLOK II KAV. 228/229, JALAN TEROGONG RAYA

Registration Date

Mar 09, 2023

Expiry Date

Jun 01, 2026

Product Type

Surgical Eye Equipment

Manual ophthalmic surgical instrument.

Non Electromedic Non Sterile

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