eudamed_udi
Primary ID: 05032384013876
POTASSIUM TELLURITE 3.5% (UDI 05032384013876)
Manufactured by Oxoid Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for POTASSIUM TELLURITE 3.5% - Primary ID 05032384013876
Device Regulatory Overview
The POTASSIUM TELLURITE 3.5% (Model/Catalog Number: SR0030J) is a medical device manufactured by Oxoid Ltd. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SR0030J
- Product Code / EMDN
- W0104010104
- Device Name
- POTASSIUM TELLURITE
- Database Sync Date
- 2026-08-09 16:46:22
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 POTASSIUM TELLURITE 3.5%?
The registered manufacturer of record for POTASSIUM TELLURITE 3.5% is Oxoid Ltd.
What is the Primary UDI-DI identifier for POTASSIUM TELLURITE 3.5%?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384013876.
What classification code is assigned to this device?
This device is registered under product classification code W0104010104.
Similar Classification Devices (W0104010104)
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