FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902052237 · Model: IPN035459 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
ARROW
Primary DI
10801902052237
Version / Model
IPN035459
Catalog Number
CDC-05531-PK1A
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-09
Public Version
5
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
e65111ce-8fa6-4adb-8786-8c04cda650d2

Device Description

ARROW(R) PICC 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
LJS Catheter,intravascular,therapeutic,long-term greater than 30 days

GMDN Terms

Code Name
36257 Peripherally-inserted central venous catheter

Identifiers

Type ID
Package 20801902052234
Primary 10801902052237

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K930129 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Excursions permitted to 15 – 30°C (59 – 86°F).