Identity
- Trade Name
- Stratus® CS Acute Care™ MYO TestPak FDA UDI
- Generic Name
- Myoglobin IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- The Stratus® CS Acute Care(TM) Myoglobin (MYO) method is an in vitro diagnostic test for the quantitative measurement of myoglobin in heparinized plasma. FDA UDI
- Model / Reference
- 10445079 FDA UDI
- Description
- The Stratus® CS Acute Care(TM) Myoglobin (MYO) method is an in vitro diagnostic test for the quantitative measurement of myoglobin in heparinized plasma. FDA UDI
Identifiers
- Catalog Number
- CMYO FDA UDI
- Primary DI / UDI-DI
- 00842768004605 FDA UDI
- 510(k) Number
- K051650 FDA UDI
- FDA Product Code
- DDR FDA UDIJHX FDA UDIJIT FDA UDIMMI FDA UDI
- GMDN Term
- Myoglobin IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5680 FDA UDI862.1215 FDA UDI862.1150 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Myoglobin IVD, kit, fluorescent immunoassay
Stratus® CS Acute Care™ MYO TestPak by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Myoglobin IVD, kit, fluorescent immunoassay.
Cleared under the same submission
K051650 also covers:
- Stratus® CS Acute Care™ CKMB CalPak — Siemens Healthcare Diagnostics
- Stratus® CS Acute Care™ CKMB DilPak — Siemens Healthcare Diagnostics
- Stratus® CS Acute Care™ CKMB TestPak — Siemens Healthcare Diagnostics
- Stratus® CS Acute Care™ MYO DilPak — Siemens Healthcare Diagnostics
- Stratus® CS Acute Care™ Myoglobin CalPak — Siemens Healthcare Diagnostics
- Stratus® CS Acute Care™ cTNI CalPak — Siemens Healthcare Diagnostics
- Stratus® CS Acute Care™ cTNI DilPak — Siemens Healthcare Diagnostics
- Stratus® CS Acute Care™ cTNI TestPak — Siemens Healthcare Diagnostics
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI fd4e53b0-29c9-4f8c-b6c7-223464c76563 37 fields · synced Jun 1, 2026