FDA UDI In Commercial Distribution 🇺🇸 United States

NIPRO SAFELET CATH

DI: 10383790006344 · Model: CI+1850 · NIPRO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
50

Basic Information

Brand Name
NIPRO SAFELET CATH
Primary DI
10383790006344
Version / Model
CI+1850
Catalog Number
CI+1850-2C
Company Name
NIPRO MEDICAL CORPORATION
Labeler DUNS
797372554
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
1cd86295-ac13-4a8c-9d06-16848b2257c8

Device Description

Intravascular catheter

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
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days

GMDN Terms

Code Name
40601 Peripheral vascular catheter

Identifiers

Type ID
Package 20383790006341
Primary 10383790006344
Package 40383790006345
Unit of Use 00383790006347

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 18 Gauge
Length 2 Inch