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Dimension Vista® ß2-Microglobulin Flex® reagent cartridge
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Dimension Vista® ß2-Microglobulin Flex® reagent cartridge FDA UDI
- Generic Name
- Beta-2-microglobulin IVD, kit, nephelometry/turbidimetry FDA UDI
- Device Name
- For the quantitative measurement of ß2-microglobulin in human serum, plasma and urine on the Dimension Vista® System FDA UDI
- Model / Reference
- 10445889 FDA UDI
- Description
- For the quantitative measurement of ß2-microglobulin in human serum, plasma and urine on the Dimension Vista® System FDA UDI
Identifiers
- Catalog Number
- K7024 FDA UDI
- Primary DI / UDI-DI
- 00842768006043 FDA UDI
- 510(k) Number
- K083463 FDA UDI
- FDA Product Code
- JZG FDA UDI
- GMDN Term
- Beta-2-microglobulin IVD, kit, nephelometry/turbidimetry FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5630 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: Beta-2-microglobulin IVD, kit, nephelometry/turbidimetry
Dimension Vista® ß2-Microglobulin Flex® reagent cartridge by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Beta-2-microglobulin IVD, kit, nephelometry/turbidimetry.
- β2-Microglobin Kit (Latex-Enhanced Immunoturbidimetric Method) — Medicalsystem Biotechnology Co., Ltd. · Class II
- Tinaquant 2Microglobulin — Roche Diagnostics Corp. · Class II
- ARCHITECT — Abbott Laboratories, Inc. · Class I
- Tinaquant ß2Microglobulin — Roche Diagnostics Corp. · Class II
- B2M AMR Fluid — The Binding Site Group · Class I
- Human Beta-2 Microglobulin Urine Kit for use on the SPAPLUS — The Binding Site Group · Class II
- Atellica CH B2M — Siemens Healthcare Diagnostics · Class II
- Optilite® Beta-2 Microglobulin Kit — The Binding Site Group · Class II
Cleared under the same submission
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 Products Ltd
Sources (1)
- FDA UDI 7c325ee6-ffe3-4f15-9f6e-732920d60588 37 fields · synced Jun 8, 2026