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JRECAN™ Clot Retriever Device - Indonesia BPOM Medical Device Registration

JRECAN™ Clot Retriever Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003420126. The device is manufactured by RICOTON TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. APT MEDICAL INDONESIA.

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
JRECAN™ Clot Retriever Device
Analysis ID: AKL 21003420126

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. APT MEDICAL INDONESIA

AR Address

Gedung APL Tower, Lantai 17 Unit T-8, Jalan Letjen S. Parman Kav.28 RT 09/ RW 05

Registration Date

Dec 10, 2024

Expiry Date

Jul 03, 2029

Product Type

Therapeutic Neurology Equipment

Neurovascular mechanical thrombectomy device for acute ischemic stroke treatment

Non Electromedic Sterile

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