FDA UDI In Commercial Distribution 🇺🇸 United States

CORFLO PEG Kit

DI: 10815149021772 · Model: 50-5020E2 · CORPAK MEDSYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CORFLO PEG Kit
Primary DI
10815149021772
Version / Model
50-5020E2
Catalog Number
50-5020E2
Company Name
CORPAK MEDSYSTEMS, INC.
Labeler DUNS
147530323
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-24
Public Version
4
Public Version Date
2020-04-20
Public Version Status
Update
Public Device Record Key
4a9f16cf-2509-48b8-9d1c-639825983cb7

Device Description

PEG Kit with ENFit connectors Pull Technique

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
KNT TUBES, GASTROINTESTINAL (AND ACCESSORIES)

GMDN Terms

Code Name
35419 Gastrostomy tube

Identifiers

Type ID
Package 20815149021779
Primary 10815149021772

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 20 French
Device Size Text, specify 20 FR (6.7mm)

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
No