FDA UDI In Commercial Distribution 🇺🇸 United States

EsoFLIP

DI: 05391530810135 · Model: ES-310 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
EsoFLIP
Primary DI
05391530810135
Version / Model
ES-310
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-16
Public Version
3
Public Version Date
2023-01-25
Public Version Status
Update
Public Device Record Key
3476681c-f63b-4c38-9144-ca7fa8e1d127

Device Description

EsoFLIP Dilation Catheter for use with EndoFLIP System

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
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
No
Sterilization Prior Use
No

Product Codes

Code Name
PIE Esophageal Dilator With Balloon And Electrode Sensors

GMDN Terms

Code Name
45712 Gastrointestinal/biliary dilation balloon catheter

Identifiers

Type ID
Package 05391530810159
Primary 05391530810135

Customer Contacts

Phone
8552767766

Device Sizes

Type Value Unit Text
Outer Diameter 20 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 25 Degrees Celsius