TELLURITE EGG YORK EMULSION (250 ML) (UDI 08435295104768)
Manufactured by Laboratorios Conda S.A.
Device Regulatory Overview
The TELLURITE EGG YORK EMULSION (250 ML) (Model/Catalog Number: 5165) 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
- 5165
- Product Code / EMDN
- W0104010104
- Device Name
- TELLURITE EGG YORK EMULSION (250 ML)
- Database Sync Date
- 2026-08-09 16:28:58
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 TELLURITE EGG YORK EMULSION (250 ML)?
The registered manufacturer of record for TELLURITE EGG YORK EMULSION (250 ML) is Laboratorios Conda S.A..
What is the Primary UDI-DI identifier for TELLURITE EGG YORK EMULSION (250 ML)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435295104768.
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.
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