FDA UDI In Commercial Distribution 🇺🇸 United States

EndoFLIP

DI: 05391530810050 · Model: EF-100 · Covidien LP
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EndoFLIP
Primary DI
05391530810050
Version / Model
EF-100
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-02
Public Version
8
Public Version Date
2023-04-21
Public Version Status
Update
Public Device Record Key
03a4359e-e2ca-4c7a-a144-d416ca18774a

Device Description

EndoFLIP System

Device Characteristics

Single Use
No
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FFX System, Gastrointestinal Motility (Electrical)

GMDN Terms

Code Name
35053 Manometric gastrointestinal motility analysis system
45569 Gastrointestinal barostat

Identifiers

Type ID
Primary 05391530810050

Customer Contacts

Phone
8582767766

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 160 KiloPascal
Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-20 – 50 Degrees Celsius