FDA UDI In Commercial Distribution 🇺🇸 United States

Alaris

DI: 20885403233446 · Model: 70200 · CAREFUSION 303, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Alaris
Primary DI
20885403233446
Version / Model
70200
Catalog Number
70200
Company Name
CAREFUSION 303, INC.
Labeler DUNS
360624720
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
70e6c5e6-4584-4414-8ca2-0b620e2d92fe

Device Description

Alaris Female Luer Lock Cap

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
Yes
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
60538 Luer/Luer linear connector, single-use

Identifiers

Type ID
Package 50885403233447
Primary 20885403233446
Unit of Use 10885403233449

Customer Contacts

Storage Conditions

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