FDA UDI
In Commercial Distribution
🇺🇸 United States
Staphaurex Plus (450 test)
DI: 05056080501529
·
Model: R30950201
·
REMEL EUROPE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Staphaurex Plus (450 test)
- Primary DI
- 05056080501529
- Version / Model
- R30950201
- Company Name
- REMEL EUROPE LIMITED
- Labeler DUNS
- 232600853
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2021-07-21
- Public Version
- 1
- Public Version Date
- 2021-07-29
- Public Version Status
- New
- Public Device Record Key
- 37fde97c-e94e-498f-84b0-61bec5591535
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| JWX | Kit, Screening, Staphylococcus Aureus | Microbiology | 866.2660 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 51659 | Staphylococcus aureus culture isolate antigen IVD, kit, agglutination | A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of antigens from Staphylococcus aureus bacteria isolated by culture from a clinical specimen, using an agglutination method. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 05056080501529 | GS1 |
Customer Contacts
- Phone
- +4401256694238
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K945538 | 000 |