eudamed_udi
Primary ID: 05032384068340
BURKHOLDERIA CEPACIA SEL. SUPP. (UDI 05032384068340)
Manufactured by Oxoid Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BURKHOLDERIA CEPACIA SEL. SUPP. - Primary ID 05032384068340
Device Regulatory Overview
The BURKHOLDERIA CEPACIA SEL. SUPP. (Model/Catalog Number: SR0189E) 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
- SR0189E
- Product Code / EMDN
- W0104010104
- Device Name
- BURKHOLDERIA CEPACIA SEL. SUPP.
- Database Sync Date
- 2026-08-09 16:29:12
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 BURKHOLDERIA CEPACIA SEL. SUPP.?
The registered manufacturer of record for BURKHOLDERIA CEPACIA SEL. SUPP. is Oxoid Ltd.
What is the Primary UDI-DI identifier for BURKHOLDERIA CEPACIA SEL. SUPP.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384068340.
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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