Identity
- Trade Name
- IMMULITE® Systems RUB CONTROL Rubella IgG FDA UDI
- Generic Name
- Rubella virus immunoglobulin G (IgG) antibody IVD, control FDA UDI
- Device Name
- Rubella IGG - IMMULITE - CTL FDA UDI
- Model / Reference
- 10469599 FDA UDI
- Description
- Rubella IGG - IMMULITE - CTL FDA UDI
Identifiers
- Catalog Number
- LRUBCM FDA UDI
- Primary DI / UDI-DI
- 00630414976730 FDA UDI
- 510(k) Number
- K963613 FDA UDI
- FDA Product Code
- LFX FDA UDI
- GMDN Term
- Rubella virus immunoglobulin G (IgG) antibody IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3510 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: Rubella virus immunoglobulin G (IgG) antibody IVD, control
IMMULITE® Systems RUB CONTROL Rubella IgG by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Rubella virus immunoglobulin G (IgG) antibody IVD, control.
- Atellica IM Rub G QC — Siemens Healthcare Diagnostics · Class II
- PreciControl Rubella IgG — Roche Diagnostics Corp. · Class I
- BioPlex 2200 — Bio-Rad Laboratories · Class I
- BioPlex 2200 — Bio-Rad Laboratories · Class II
- Validate — LGC Clinical Diagnostics, Inc. · Class I
- LIAISON® Rubella IgG TRI-Controls — Diasorin Inc.
- BioPlex 2200 — Bio-Rad Laboratories · Class I
- ADVIA Centaur® Rub G QC — Siemens Healthcare Diagnostics · 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 76d45c31-bd54-4fec-a16b-1f19f74eb21f 37 fields · synced May 30, 2026