eudamed_udi
Primary ID: 05032384011728
PSEUDOMONAS C-F-C SELECTIVE SUPPLEMENT (UDI 05032384011728)
Manufactured by Oxoid Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PSEUDOMONAS C-F-C SELECTIVE SUPPLEMENT - Primary ID 05032384011728
Device Regulatory Overview
The PSEUDOMONAS C-F-C SELECTIVE SUPPLEMENT (Model/Catalog Number: SR0103E) 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
- SR0103E
- Product Code / EMDN
- W0104010104
- Device Name
- PSEUDOMONAS C-F-C SELECTIVE SUPPLEMENT
- Database Sync Date
- 2026-08-09 16:58:41
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 PSEUDOMONAS C-F-C SELECTIVE SUPPLEMENT?
The registered manufacturer of record for PSEUDOMONAS C-F-C SELECTIVE SUPPLEMENT is Oxoid Ltd.
What is the Primary UDI-DI identifier for PSEUDOMONAS C-F-C SELECTIVE SUPPLEMENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384011728.
What classification code is assigned to this device?
This device is registered under product classification code W0104010104.
Similar Classification Devices (W0104010104)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint