Identity
- Trade Name
- VIDAS® RUB IgG FDA UDI
- Generic Name
- Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- VIDAS ® RUB IgG (RBG) assay is a quantitative IA intended for use on VIDAS family instrument in the determination of IgG antibodies to rubella virus in human serum. FDA UDI
- Model / Reference
- 30226 FDA UDI
- Description
- VIDAS ® RUB IgG (RBG) assay is a quantitative IA intended for use on VIDAS family instrument in the determination of IgG antibodies to rubella virus in human serum. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03573026138585 FDA UDI
- 510(k) Number
- K141133 FDA UDI
- FDA Product Code
- LFX FDA UDI
- GMDN Term
- Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) 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
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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, kit, enzyme immunoassay (EIA)
VIDAS® RUB IgG by Biomerieux , Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA).
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Cleared under the same submission
K141133 also covers:
- VIDAS 3 — BIOMERIEUX , INC.
- VIDAS 3 — BIOMERIEUX , INC.
- VIDAS® 3 — BIOMERIEUX , INC.
- VIDAS® 3 ASSAY DILUTION CUP — BIOMERIEUX , INC.
- VIDAS® 3 SOFTWARE V1.4 — BIOMERIEUX , INC.
- VIDAS® D-Dimer Exclusion II ™ — BIOMERIEUX , INC.
- VIDAS® H. pylori IgG — BIOMERIEUX , INC.
- VIDAS® HCG — BIOMERIEUX , INC.
- VIDAS® Refurbished — BIOMERIEUX , INC.
- VIDAS® TOXO IgM — BIOMERIEUX , INC.
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
- Biomerieux , Inc.
Sources (1)
- FDA UDI 968144e9-630c-4fb4-82cc-a521239db6a6 35 fields · synced Jun 8, 2026