FDA UDI In Commercial Distribution 🇺🇸 United States

MeriSite (TM)

DI: 00810083350868 · Model: MHI-MSI · Sensimedical LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MeriSite (TM)
Primary DI
00810083350868
Version / Model
MHI-MSI
Catalog Number
MHI-MSI
Company Name
Sensimedical LLC
Labeler DUNS
117526048
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-04
Public Version
1
Public Version Date
2024-01-12
Public Version Status
New
Public Device Record Key
531bbfe0-0a8e-45c1-97f2-752c813af380

Device Description

MeriSite (TM) 300 psi High-Pressure Needleless Neutral Valve

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
No

Product Codes

Code Name
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 00810083350875
Primary 00810083350868
Package 00810083350882

Premarket Submissions

Submission Number Supplement Number
K121511 000