Identity
- Trade Name
- Hemastix® Reagent Strips FDA UDI
- Generic Name
- Urine blood IVD, kit, rapid colorimetric, clinical FDA UDI
- Device Name
- HEMASTIX® is a firm plastic strip to which is affixed a reagent area that tests for occult blood in urine. Test results may provide information on urinary tract status. FDA UDI
- Model / Reference
- 10312568 FDA UDI
- Description
- HEMASTIX® is a firm plastic strip to which is affixed a reagent area that tests for occult blood in urine. Test results may provide information on urinary tract status. FDA UDI
Identifiers
- Catalog Number
- A2190B16 FDA UDI
- Primary DI / UDI-DI
- 00630414550596 FDA UDI
- 510(k) Number
- K905396 FDA UDI
- FDA Product Code
- JIO FDA UDI
- GMDN Term
- Urine blood IVD, kit, rapid colorimetric, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.6550 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: Urine blood IVD, kit, rapid colorimetric, clinical
Hemastix® Reagent Strips by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K905396 also covers:
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 c2d28258-da85-4480-9967-f4430c40bb76 37 fields · synced May 30, 2026