gudid
Primary ID: SEN-V2000
Mespere (UDI SEN-V2000)
Manufactured by Mespere LifeSciences Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mespere - Primary ID SEN-V2000
Device Regulatory Overview
The Mespere (Model/Catalog Number: SEN-V2000) is a medical device manufactured by Mespere LifeSciences Inc. This product is indexed under FDA Product Code / Category Classification PFA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SEN-V2000
- Product Code / EMDN
- PFA
- Device Name
- Database Sync Date
- 2026-08-09 09:53:47
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 Mespere?
The registered manufacturer of record for Mespere is Mespere LifeSciences Inc.
What is the Primary UDI-DI identifier for Mespere?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SEN-V2000.
What classification code is assigned to this device?
This device is registered under product classification code PFA.
Similar Classification Devices (PFA)
Other Devices by Mespere LifeSciences Inc
Programmatic Export
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JSON API Endpoint