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SURU Ureteral Stent Kit (Double J Stent) - Indonesia BPOM Medical Device Registration

SURU Ureteral Stent Kit (Double J Stent) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804910726. The device is manufactured by SURU INTERNATIONAL PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SUCCESS WITH DAVID.

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 : C
SURU Ureteral Stent Kit (Double J Stent)
Analysis ID: AKL 20804910726

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. SUCCESS WITH DAVID

AR Address

GEDUNG NUCIRA LANTAI 3 JL. MT. HARYONO KAV. 27 KEL. TEBET TIMUR

Registration Date

Feb 15, 2019

Expiry Date

Dec 31, 2023

Product Type

Gastroenterology-Surgical Urology Equipment

Ureteral stent.

Non Electromedic Sterile

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