FDA UDI In Commercial Distribution 🇺🇸 United States

Medline Industries, Inc.

DI: 10889942017959 · Model: DYKM1212 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline Industries, Inc.
Primary DI
10889942017959
Version / Model
DYKM1212
Catalog Number
DYKM1212
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-07
Public Version
5
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
eda5c5de-47bc-4517-9374-2b1a1f83793f

Device Description

PATIENT MONITOR KIT

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRS TRANSDUCER, BLOOD-PRESSURE, EXTRAVASCULAR

GMDN Terms

Code Name
44058 General surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 10889942017959

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K061573 000