Identity
- Trade Name
- Stratus® CS Acute Care™ MYO DilPak FDA UDI
- Generic Name
- Myoglobin IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- The Stratus® CS Acute Care(TM) Myoglobin Dilution Pak (MYO DilPak) is an in vitro diagnostic product intended to be used in conjunction with the Acute Care(TM) MYO TestPak for the measurement of samples with elevated levels of Myoglobin. FDA UDI
- Model / Reference
- 10445081 FDA UDI
- Description
- The Stratus® CS Acute Care(TM) Myoglobin Dilution Pak (MYO DilPak) is an in vitro diagnostic product intended to be used in conjunction with the Acute Care(TM) MYO TestPak for the measurement of samples with elevated levels of Myoglobin. FDA UDI
Identifiers
- Catalog Number
- CMYO-D FDA UDI
- Primary DI / UDI-DI
- 00842768004629 FDA UDI
- 510(k) Number
- K051650 FDA UDI
- FDA Product Code
- JHX FDA UDIMMI FDA UDIDDR FDA UDIJIT FDA UDI
- GMDN Term
- Myoglobin IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1215 FDA UDI866.5680 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 DilPak 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 TestPak — 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 |
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Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI 2690e15a-6e0f-484c-bc52-1041fd991472 37 fields · synced May 31, 2026