FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 00080196750118 · Model: MDT5000 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
MEDLINE
Primary DI
00080196750118
Version / Model
MDT5000
Catalog Number
MDT5000
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-25
Public Version
1
Public Version Date
2025-01-02
Public Version Status
New
Public Device Record Key
11cd122d-3ed5-48bb-a048-ee7ed0b4503c

Device Description

ALARM,ADVANTAGE,MAGNETIC TETHER

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
KMI MONITOR, BED PATIENT

GMDN Terms

Code Name
30087 Vulnerable patient home alert system

Identifiers

Type ID
Package 40080196750116
Primary 00080196750118

Customer Contacts