FDA UDI In Commercial Distribution 🇺🇸 United States

Medex

DI: 10351688508669 · Model: MX20880 · SMITHS MEDICAL ASD, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medex
Primary DI
10351688508669
Version / Model
MX20880
Company Name
SMITHS MEDICAL ASD, INC.
Labeler DUNS
828611934
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-30
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
be931859-73ed-413b-ae1d-2a046f10be65

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
DPT PROBE, BLOOD-FLOW, EXTRAVASCULAR
KRA Catheter, continuous flush

GMDN Terms

Code Name
35927 Invasive-pressure external transducer, single-use

Identifiers

Type ID
Package 50351688508667
Primary 10351688508669

Premarket Submissions

Submission Number Supplement Number
K790455 000
K942377 000