Peru DIGEMID registration DMDIV3632E

UREA-[13 C] CAPSULE BREATH TEST KIT.

Peru·IN VITRO MEDICAL DEVICE·SHENZHEN ZHONGHE HEADWAY BIO-SCI & TECH CO., LTD.·Registered November 23, 2020

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV3632E
Registration Date: November 23, 2020
Expiration Date: November 23, 2025
Creation Date: March 10, 2025

Manufacturer

Name: SHENZHEN ZHONGHE HEADWAY BIO-SCI & TECH CO., LTD.

Authorized Representative

Name: HOSPICARE S.A.C.

About this record

Access comprehensive regulatory information for UREA-[13 C] CAPSULE BREATH TEST KIT. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV3632E and manufactured by SHENZHEN ZHONGHE HEADWAY BIO-SCI & TECH CO., LTD.. The device was registered on November 23, 2020.

This page provides complete registration details including product type (IN VITRO MEDICAL DEVICE), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.