FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10080196990320 · Model: DYND12578 · MEDLINE INDUSTRIES, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10080196990320
Version / Model
DYND12578
Catalog Number
DYND12578
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-14
Public Version
5
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
da7c7fde-d78b-4847-a0ed-506318dbb647

Device Description

BAG,LEG,TWIST-VALVE,STRAPS,LARGE,32OZ

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KNX COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER
FAQ BAG, URINE COLLECTION, LEG, FOR EXTERNAL USE, STERILE

GMDN Terms

Code Name
58923 Wearable adult urine collection bag, open-ended

Identifiers

Type ID
Package 30080196990324
Primary 10080196990320

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Label does not mention Storage Conditions