cobas b 221 GLU/LAC/UREA (BUN) Cassette (UDI 03261085184)
Manufactured by Roche Diagnostics GmbH
Device Regulatory Overview
The cobas b 221 GLU/LAC/UREA (BUN) Cassette (Model/Catalog Number: 03261085184) is a medical device manufactured by Roche Diagnostics GmbH. This product is indexed under FDA Product Code / Category Classification CDS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03261085184
- Product Code / EMDN
- CDS
- Device Name
- Database Sync Date
- 2026-08-09 09:33:50
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 cobas b 221 GLU/LAC/UREA (BUN) Cassette?
The registered manufacturer of record for cobas b 221 GLU/LAC/UREA (BUN) Cassette is Roche Diagnostics GmbH.
What is the Primary UDI-DI identifier for cobas b 221 GLU/LAC/UREA (BUN) Cassette?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03261085184.
What classification code is assigned to this device?
This device is registered under product classification code CDS.
Similar Classification Devices (CDS)
Other Devices by Roche Diagnostics GmbH
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