FRASER LISTERIA SELECTIVE SUPPLEMENT (UDI 08435295180151)
Manufactured by Laboratorios Conda S.A.
Device Regulatory Overview
The FRASER LISTERIA SELECTIVE SUPPLEMENT (Model/Catalog Number: 6001) is a medical device manufactured by Laboratorios Conda S.A.. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6001
- Product Code / EMDN
- W0104010104
- Device Name
- FRASER LISTERIA SELECTIVE SUPPLEMENT
- Database Sync Date
- 2026-08-09 16:54:34
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of FRASER LISTERIA SELECTIVE SUPPLEMENT?
The registered manufacturer of record for FRASER LISTERIA SELECTIVE SUPPLEMENT is Laboratorios Conda S.A..
What is the Primary UDI-DI identifier for FRASER LISTERIA SELECTIVE SUPPLEMENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435295180151.
What classification code is assigned to this device?
This device is registered under product classification code W0104010104.
Similar Classification Devices (W0104010104)
Other Devices by Laboratorios Conda S.A.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint