FDA UDI In Commercial Distribution 🇺🇸 United States

EndoFLIP

DI: 05391530810012 · Model: EF-322N · Covidien LP
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
EndoFLIP
Primary DI
05391530810012
Version / Model
EF-322N
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
2023-10-02
Public Version Status
Update
Public Device Record Key
bb52ca1b-06df-4de0-a1df-3bf98b88e97f

Device Description

ENDO CATHETER EF-322N 16CM NASAL TIP

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
FFX System, Gastrointestinal Motility (Electrical)

GMDN Terms

Code Name
35053 Manometric gastrointestinal motility analysis system
45569 Gastrointestinal barostat

Identifiers

Type ID
Primary 05391530810012
Package 05391530810074

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 25 Degrees Celsius