FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902116038 · Model: IPN036588 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
ARROW
Primary DI
10801902116038
Version / Model
IPN036588
Catalog Number
ASK-42854-PRR
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
11
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
dbc0d255-d6e5-4af0-b7c3-f8de3b0df4ce

Device Description

Pressure Injectable Arrowg+ard Blue Plus(R) Four-Lumen CVC Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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
61594 Central venous catheterization kit, short-term

Identifiers

Type ID
Package 40801902116039
Primary 10801902116038

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071538 000