FDA UDI In Commercial Distribution 🇺🇸 United States

Transpac™

DI: 00887709061828 · Model: 46112-13 · ICU MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Transpac™
Primary DI
00887709061828
Version / Model
46112-13
Catalog Number
46112-13
Company Name
ICU MEDICAL, INC.
Labeler DUNS
118380146
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-28
Public Version
1
Public Version Date
2021-08-05
Public Version Status
New
Public Device Record Key
e44cf7e1-4ff5-49f1-9ebc-362d7389877c

Device Description

Transpac™ IT Monitoring Kit w/Arterial 84" Safeset™ Reservoir, 3ml Flush Device and Needleless Valves

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DRS Transducer, blood-pressure, extravascular

GMDN Terms

Code Name
45275 Invasive blood pressure transducer set

Identifiers

Type ID
Package 10887709061825
Primary 00887709061828

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K052828 000