FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902130423 · Model: IPN037693 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902130423
Version / Model
IPN037693
Catalog Number
ASK-45854-PECL1
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-30
Public Version
15
Public Version Date
2023-10-25
Public Version Status
Update
Public Device Record Key
83f6c5a6-909a-4526-80a0-4f896aef4dd1

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
34842 Epidural anaesthesia set, non-medicated

Identifiers

Type ID
Package 20801902130420
Primary 10801902130423

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071538 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius