FDA UDI In Commercial Distribution 🇺🇸 United States

Ameritus

DI: 10817522012223 · Model: AEG-Y80P-80 · KENTEC MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Ameritus
Primary DI
10817522012223
Version / Model
AEG-Y80P-80
Catalog Number
AEG-Y80P-80
Company Name
KENTEC MEDICAL, INC.
Labeler DUNS
066175613
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-09
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
99b78b9f-45d6-4d31-8a18-dac4b08d22fb

Device Description

8fr 80cm dual port feeding tube

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
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FPD Tube, Feeding

GMDN Terms

Code Name
38561 Nasogastric/orogastric tube

Identifiers

Type ID
Package 30817522012227
Primary 10817522012223
Package 20817522012220

Customer Contacts

Phone
949-863-0810

Premarket Submissions

Submission Number Supplement Number
K100526 000