FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10080196031252 · Model: DYND13520 · MEDLINE INDUSTRIES, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10080196031252
Version / Model
DYND13520
Catalog Number
DYND13520
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
a831b080-78f4-4ae6-ada6-32f718695bf6

Device Description

CATHETER,URETHRAL,REDRUBBER,STERILE,20FR

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
No

Product Codes

Code Name
KOD CATHETER, UROLOGICAL
EZL CATHETER, RETENTION TYPE, BALLOON

GMDN Terms

Code Name
31975 Urethral/ureteral catheter connector, sterile

Identifiers

Type ID
Package 40080196031253
Primary 10080196031252

Customer Contacts

Storage Conditions

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