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Sterile Hypodermic Syringes for Single Use (with Needles) - EUDAMED Registration 06924164700399

Access comprehensive regulatory information for Sterile Hypodermic Syringes for Single Use (with Needles) in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 06924164700399 and manufactured by Jiangyin Jinfeng Medical Equipment CO., Ltd. in China.

This page provides complete registration details including trade name (Sterile Hypodermic Syringes for Single Use (with Needles)20ml), manufacturer information, authorized representative details, competent authority (Agencia Espaรฑola de Medicamentos y Productos Sanitarios), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.

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EUDAMED Official Data
Class IIa
06924164700399
No
Sterile Hypodermic Syringes for Single Use (with Needles)
Trade Name: Sterile Hypodermic Syringes for Single Use (with Needles)20ml
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Device Description (EMDN)

INFUSION AND IRRIGATION SYRINGES, 2-PIECE LUER CONE, 2-PIECE WITH NEEDLE, SINGLE-USE

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
A020102010101
Trade Name
Sterile Hypodermic Syringes for Single Use (with Needles)20ml
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06924164700399
Basic UDI
69241647jf003YK
Version Date
December 17, 2023
Manufacturer Last Update
November 23, 2021
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No. 74 Zhoujia Village, Jinfeng Village, Xuxiake Town, 214407 Jiangyin, Peopleโ€™s Republic of China Wuxi
Email
39896066@qq.com
Authorized Representative
SRN
DE-AR-000007996
Country
Germany
Address
11 Koenigsberger Strasse Muenster Hessen
Email
contact@glgi.de
Telephone
004960714977513
Regulatory Information
Competent Authority
Agencia Espaรฑola de Medicamentos y Productos Sanitarios
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Device Characteristics
Human Tissues
No
Animal Tissues
No