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RUBY SC Pre Dilatation Catheter - Indonesia BPOM Medical Device Registration

RUBY SC Pre Dilatation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505420087. The device is manufactured by MULTIMEDICS. LLP from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. INDOMED PHARMA.

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
RUBY SC Pre Dilatation Catheter
Analysis ID: AKL 30505420087

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MULTIMEDICS. LLP

Country of Origin

India

Authorized Representative

PT. INDOMED PHARMA

AR Address

Kelapa Gading Hyper Mall, Lantai Dasar Blok B10 No. 03 (DB1003), Jakarta Utara

Registration Date

Jul 11, 2024

Expiry Date

Aug 29, 2028

Product Type

Therapeutic Cardiology Equipment

Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter

Non Electromedic Sterile

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