FDA UDI In Commercial Distribution 🇺🇸 United States

VersaSafe

DI: 27613203033613 · Model: 9391-0200 · CAREFUSION 303, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
45

Basic Information

Brand Name
VersaSafe
Primary DI
27613203033613
Version / Model
9391-0200
Catalog Number
9391-0200
Company Name
CAREFUSION 303, INC.
Labeler DUNS
360624720
Distribution Status
In Commercial Distribution
Device Count in Pkg
45
Record Status
Published
Publish Date
2016-09-22
Public Version
4
Public Version Date
2020-04-27
Public Version Status
Update
Public Device Record Key
0d1cfa2d-f53d-44a9-8f85-f58daea3cc5c

Device Description

VersaSafe Plastic Cannula

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
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
FPA Set, administration, intravascular

GMDN Terms

Code Name
42631 Split-septum needleless valve-connector

Identifiers

Type ID
Package 37613203009523
Primary 27613203033613
Unit of Use 07613203009515

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 125 Degrees Fahrenheit