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MEDNOVA Single Use Hemoclips - Indonesia BPOM Medical Device Registration

MEDNOVA Single Use Hemoclips is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804420077. The device is manufactured by ZHEJIANG CHUANGXIANG MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is EDISON AMBASSADOR MEANS.

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
MEDNOVA Single Use Hemoclips
Analysis ID: AKL 20804420077

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

EDISON AMBASSADOR MEANS

AR Address

Jl. Oasis Sememi Raya No. 1 RT 05 RW 04, Kel. Sememi, Kec. Benowo, Surabaya, Jawa Timur

Registration Date

Jul 02, 2024

Expiry Date

Jul 23, 2028

Product Type

Gastroenterology-Surgical Urology Equipment

Endoscopic electrosurgical unit and accessories.

Non Electromedic Sterile

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