FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10080196030903 · Model: DYND12302 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10080196030903
Version / Model
DYND12302
Catalog Number
DYND12302
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
38df8847-8ccb-42c3-9338-b0c9b623a3fb

Device Description

CATHETER,EXTERNAL,MALE,EXO,LTX,MED,30MM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
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
NNX DEVICE, INCONTINENCE, UROSHEATH TYPE, NON-STERILE

GMDN Terms

Code Name
32089 Cystographic/urethrographic catheter, male

Identifiers

Type ID
Package 40080196030904
Primary 10080196030903

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Protect from freezing, avoid excessive heat