FDA UDI In Commercial Distribution 🇺🇸 United States

Rempress

DI: 04560138481004 · Model: 100 · NEMOTO KYORINDO CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Rempress
Primary DI
04560138481004
Version / Model
100
Company Name
NEMOTO KYORINDO CO.,LTD.
Labeler DUNS
692691710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
0e06183f-281b-4003-bd61-6af1579f3fc8

Device Description

Nemoto Rempress contrast delivery system for angiography, pedestal type unit.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXT Injector And Syringe, Angiographic

GMDN Terms

Code Name
57997 Angiography contrast medium injection system, line-powered, mobile

Identifiers

Type ID
Primary 04560138481004
Package 14560138481001

Premarket Submissions

Submission Number Supplement Number
K092896 000

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius