FDA UDI In Commercial Distribution 🇺🇸 United States

Medline Industries, Inc.

DI: 10889942428472 · Model: DYNJ53310 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline Industries, Inc.
Primary DI
10889942428472
Version / Model
DYNJ53310
Catalog Number
DYNJ53310
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-30
Public Version
8
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
ac2db7c4-723f-4cd1-99fe-2ecd297c8bb8

Device Description

KFMH JEDDAH DIAGNOSTIC PACK

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
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OES Cardiac catheterization kit

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 10889942428472
Package 40889942428473

Customer Contacts