N LATEX FLC lambda 10873630
by Siemens Healthcare Diagnostics Products Ltd
N LATEX FLC lambda 10873630 (OPJB07) is a Class II device made by Siemens Healthcare Diagnostics Products Ltd, listed in FDA GUDID since 28 Jan 2018 (UDI-DI 00630414167664), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00630414167664 | Date28 Jan 2018 | StatusListed |
Official records
- AccessGUDID record 00630414167664
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- N LATEX FLC lambda
- Generic name
- Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry
- Model / Ref / Catalog
- 10873630, OPJB07
- Primary DI / UDI-DI
- 00630414167664
- FDA product code
- DEH
- GMDN term
- Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry
- Device class
- Class II
- Regulation number
- 866.5550
- GUDID distribution status
- In Commercial Distribution
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