FDA UDI In Commercial Distribution 🇺🇸 United States

AVANOS

DI: 00350770915227 · Model: 91522 · Avanos Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Basic Information

Brand Name
AVANOS
Primary DI
00350770915227
Version / Model
91522
Catalog Number
91522
Company Name
Avanos Medical, Inc.
Labeler DUNS
079375431
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2020-05-23
Public Version
3
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
d36df9bf-ec0a-4d08-9c18-406448d9ae01

Device Description

Enteral Access Dilation System

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KGC TUBE, GASTRO-ENTEROSTOMY

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Unit of Use 10350770915224
Primary 00350770915227

Customer Contacts