FDA UDI In Commercial Distribution 🇺🇸 United States

Staphaurex Plus (150 test)

DI: 05056080501512 · Model: R30950102 · REMEL EUROPE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Staphaurex Plus (150 test)
Primary DI
05056080501512
Version / Model
R30950102
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
e345caf1-767e-4cba-bf91-7ea6c8b775b1

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
JWX Kit, Screening, Staphylococcus Aureus

GMDN Terms

Code Name
51659 Staphylococcus aureus culture isolate antigen IVD, kit, agglutination

Identifiers

Type ID
Primary 05056080501512

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K945538 000