FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10193489105780 · Model: DYND30212B · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10193489105780
Version / Model
DYND30212B
Catalog Number
DYND30212B
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-17
Public Version
1
Public Version Date
2022-02-25
Public Version Status
New
Public Device Record Key
27811dc0-48d6-44e2-b24c-620da7ef81e5

Device Description

KIT,MIDSTREAM,FUNNEL,BZK,3OZ,CLICK,PREM

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
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
OIE Urine collection kit (excludes HIV testing)

GMDN Terms

Code Name
65196 General specimen collection kit

Identifiers

Type ID
Package 20193489105787
Primary 10193489105780

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature.