GUDIDData
eudamed_udi Primary ID: 06949236212235

Sterile Syringes for Single Use (UDI 06949236212235)

Manufactured by Berpu Medical Technology Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sterile Syringes for Single Use - Primary ID 06949236212235

Device Regulatory Overview

The Sterile Syringes for Single Use (Model/Catalog Number: L103) is a medical device manufactured by Berpu Medical Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification A020102020102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
L103
Product Code / EMDN
A020102020102
Device Name
Sterile Syringes for Single Use
Database Sync Date
2026-08-09 16:49:34

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Sterile Syringes for Single Use?

The registered manufacturer of record for Sterile Syringes for Single Use is Berpu Medical Technology Co., Ltd.

What is the Primary UDI-DI identifier for Sterile Syringes for Single Use?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06949236212235.

What classification code is assigned to this device?

This device is registered under product classification code A020102020102.

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