Pure Global

ClearPetra Ureteral Stent - Indonesia BPOM Medical Device Registration

ClearPetra Ureteral Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804320292. The device is manufactured by WELL LEAD MEDICAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SOMETECH NEW Zealand.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
ClearPetra Ureteral Stent
Analysis ID: AKL 20804320292

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

SOMETECH NEW Zealand

AR Address

AKR Tower Lantai 11 Unit 11G, Jl. Panjang No. 5

Registration Date

Jun 13, 2023

Expiry Date

Dec 07, 2027

Product Type

Gastroenterology-Surgical Urology Equipment

Ureteral stent.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing