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ANGIODIN-PROCTO Medical Equipment for Hemorrhoids Treatment - Indonesia BPOM Medical Device Registration

ANGIODIN-PROCTO Medical Equipment for Hemorrhoids Treatment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804917577. The device is manufactured by AO NPF 'BIOSS" from Russia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. EUREKA ETERNAL SUCCESS.

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 : B
ANGIODIN-PROCTO Medical Equipment for Hemorrhoids Treatment
Analysis ID: AKL 20804917577

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AO NPF 'BIOSS"

Country of Origin

Russia

Authorized Representative

PT. EUREKA ETERNAL SUCCESS

AR Address

Jl. pantai Indah Barat Komplek Toho Blok B No. 21 Rt/Rw 001/003 Kelurahan Muara Kamal Kec. Penjaringan Jakarta Utara

Registration Date

Jul 16, 2022

Expiry Date

Jun 30, 2027

Product Type

Gastroenterology-Surgical Urology Equipment

Hemorrhoidal ligator.

Non Radiation Electromedics

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