GUDIDData
gudid Primary ID: Rigid, Dark blue, LP0302PF

Inoculating Needle Rigid perforated bag packTypenex LP0302PF (UDI Rigid, Dark blue, LP0302PF)

Manufactured by ZHEJIANG RUNLAB TECHNOLOGY CO., LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Inoculating Needle Rigid perforated bag packTypenex LP0302PF - Primary ID Rigid, Dark blue, LP0302PF

Device Regulatory Overview

The Inoculating Needle Rigid perforated bag packTypenex LP0302PF (Model/Catalog Number: Rigid, Dark blue, LP0302PF) is a medical device manufactured by ZHEJIANG RUNLAB TECHNOLOGY CO., LTD. This product is indexed under FDA Product Code / Category Classification LIB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Rigid, Dark blue, LP0302PF
Product Code / EMDN
LIB
Device Name
Inoculating Needle Rigid perforated bag packTypenex LP0302PF
Database Sync Date
2026-08-09 09:06:39

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 Inoculating Needle Rigid perforated bag packTypenex LP0302PF?

The registered manufacturer of record for Inoculating Needle Rigid perforated bag packTypenex LP0302PF is ZHEJIANG RUNLAB TECHNOLOGY CO., LTD.

What is the Primary UDI-DI identifier for Inoculating Needle Rigid perforated bag packTypenex LP0302PF?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Rigid, Dark blue, LP0302PF.

What classification code is assigned to this device?

This device is registered under product classification code LIB.

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