← Back to catalogue
Syva® Emit® 2000 Cyclosporine Specific Negative Calibrator
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Syva® Emit® 2000 Cyclosporine Specific Negative Calibrator FDA UDI
- Generic Name
- Cyclosporin A/cyclosporine therapeutic drug monitoring IVD, control FDA UDI
- Device Name
- Emit ® 2000 Cyclosporine Specific Negative Calibrator FDA UDI
- Model / Reference
- 10445377 FDA UDI
- Description
- Emit ® 2000 Cyclosporine Specific Negative Calibrator FDA UDI
Identifiers
- Catalog Number
- 6R319UL FDA UDI
- Primary DI / UDI-DI
- 00842768001475 FDA UDI
- PMA Number
- P920031 FDA UDI
- FDA Product Code
- MKW FDA UDI
- GMDN Term
- Cyclosporin A/cyclosporine therapeutic drug monitoring IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1235 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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: Cyclosporin A/cyclosporine therapeutic drug monitoring IVD, control
Syva® Emit® 2000 Cyclosporine Specific Negative Calibrator by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Cyclosporin A/cyclosporine therapeutic drug monitoring IVD, control.
- ADVIA Centaur® CsA MCM — Siemens Healthcare Diagnostics · Class I
- Atellica IM CsA MCM — Siemens Healthcare Diagnostics · Class I
Cleared under the same submission
P920031 also covers:
- CSAII Cyclosporine II — Roche Diagnostics Corp.
- Cyclosporine Calibrator 0 ng/mL — Roche Diagnostics Corp.
- Cyclosporine Calibrators — Roche Diagnostics Corp.
- Syva® Emit® 2000 Cyclosporine Specific Calibrators — Siemens Healthcare Diagnostics
- Syva® Emit® Cyclosporine Pretreatment Reagent — 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 20d112dc-b7dc-49f5-8e3d-ef11c5d8c619 37 fields · synced Jun 8, 2026