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Sterile Hypodermic syringe for single use - EUDAMED Registration 08906067661500

Access comprehensive regulatory information for Sterile Hypodermic syringe for single use 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 08906067661500 and manufactured by Lifelong Meditech Private Limited in India.

This page provides complete registration details including trade name (Lifelong Matrix), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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
08906067661500
No
Sterile Hypodermic syringe for single use
Trade Name: Lifelong Matrix
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Device Description (EMDN)

SYRINGES, SINGLE-USE - OTHER

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
A020199
Trade Name
Lifelong Matrix
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
08906067661500
Basic UDI
B-08906067661500
Version Date
August 28, 2023
Manufacturer Last Update
September 29, 2021
Active Status
No
Manufacturer
Country
India
Country Type
NON_EU
Address
Plot No. 18, Sector-5, IMT, Manesar, Gurgaon Haryana
Email
Hsrivastava@lifelongindia.com
Authorized Representative
SRN
NL-AR-000000594
Country
Netherlands
Address
Keizersgracht 482 Amsterdam
Email
nk@meddevices.net
Telephone
+31202254558
Regulatory Information
Competent Authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable Legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed On The Market
France
Market Available
France:2022-08-10~2023-07-08
Device Characteristics
Human Tissues
No
Animal Tissues
No