gudid
Primary ID: 2040
Precision Syringe (UDI 2040)
Manufactured by VITALOGRAPH (IRELAND) LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Precision Syringe - Primary ID 2040
Device Regulatory Overview
The Precision Syringe (Model/Catalog Number: 2040) is a medical device manufactured by VITALOGRAPH (IRELAND) LIMITED. This product is indexed under FDA Product Code / Category Classification BXW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2040
- Product Code / EMDN
- BXW
- Device Name
- 2040 PRECISION SYRINGE 1 LITRE
- Database Sync Date
- 2026-08-09 09:22:51
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Precision Syringe?
The registered manufacturer of record for Precision Syringe is VITALOGRAPH (IRELAND) LIMITED.
What is the Primary UDI-DI identifier for Precision Syringe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2040.
What classification code is assigned to this device?
This device is registered under product classification code BXW.
Similar Classification Devices (BXW)
Other Devices by VITALOGRAPH (IRELAND) LIMITED
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