The Rapidlab 1265 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites and CO-oximetry in arterial, venous and capillary whole blood samples. (UDI Z-1962-2015)
Manufactured by Siemens Healthcare Diagnostics, Inc
Device Regulatory Overview
The The Rapidlab 1265 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites and CO-oximetry in arterial, venous and capillary whole blood samples. (Model/Catalog Number: Unspecified) is a medical device manufactured by Siemens Healthcare Diagnostics, Inc. This product is indexed under FDA Product Code / Category Classification Siemens Material Number (SMN): 10321852, 10470366, 10491395, 10335524 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- Siemens Material Number (SMN): 10321852, 10470366, 10491395, 10335524
- Device Name
- The Rapidlab 1265 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites and CO-oximetry in arterial, venous and capillary whole blood samples.
- Database Sync Date
- 2026-08-09 10:06:40
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 The Rapidlab 1265 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites and CO-oximetry in arterial, venous and capillary whole blood samples.?
The registered manufacturer of record for The Rapidlab 1265 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites and CO-oximetry in arterial, venous and capillary whole blood samples. is Siemens Healthcare Diagnostics, Inc.
What is the Primary UDI-DI identifier for The Rapidlab 1265 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites and CO-oximetry in arterial, venous and capillary whole blood samples.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-1962-2015.
What classification code is assigned to this device?
This device is registered under product classification code Siemens Material Number (SMN): 10321852, 10470366, 10491395, 10335524.
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