FDA UDI In Commercial Distribution 🇺🇸 United States

Careflow™

DI: 10884450321505 · Model: 10884450321505 · ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Careflow™
Primary DI
10884450321505
Version / Model
10884450321505
Catalog Number
681631/A
Company Name
ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.
Labeler DUNS
595138793
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-09-20
Public Version
1
Public Version Date
2022-09-28
Public Version Status
New
Public Device Record Key
87fcc87a-f99e-4b79-9f01-2967403a9550

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
FOZ Catheter, intravascular, therapeutic, short-term less than 30 days

GMDN Terms

Code Name
64575 Peripheral artery cannula

Identifiers

Type ID
Package 20884450321502
Primary 10884450321505
Unit of Use 00884450321508

Device Sizes

Type Value Unit Text
Device Size Text, specify Lumens-1 Lumen
Device Size Text, specify French Size (F)-2.5F
Device Size Text, specify Length-60 mm