eudamed_udi
Primary ID: 05032384128921
KIMMIG MEDIUM (UDI 05032384128921)
Manufactured by Oxoid Deutschland GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KIMMIG MEDIUM - Primary ID 05032384128921
Device Regulatory Overview
The KIMMIG MEDIUM (Model/Catalog Number: PO5019A) is a medical device manufactured by Oxoid Deutschland GmbH. This product is indexed under FDA Product Code / Category Classification W0104030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PO5019A
- Product Code / EMDN
- W0104030201
- Device Name
- KIMMIG MEDIUM
- Database Sync Date
- 2026-08-09 16:58:59
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 KIMMIG MEDIUM?
The registered manufacturer of record for KIMMIG MEDIUM is Oxoid Deutschland GmbH.
What is the Primary UDI-DI identifier for KIMMIG MEDIUM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384128921.
What classification code is assigned to this device?
This device is registered under product classification code W0104030201.
Similar Classification Devices (W0104030201)
Other Devices by Oxoid Deutschland GmbH
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