FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10888277362444 · Model: MDS88200DLB · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10888277362444
Version / Model
MDS88200DLB
Catalog Number
MDS88200DLB
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-22
Public Version
2
Public Version Date
2021-11-23
Public Version Status
Update
Public Device Record Key
f4d02592-4288-42b1-8a16-581f61f65ef3

Device Description

LIFT,PATIENT,HYDRAULIC, LOW BASE

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Yes
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
FSA Lift, patient, non-ac-powered

GMDN Terms

Code Name
45678 Mobile patient lifting system, manual

Identifiers

Type ID
Primary 10888277362444

Customer Contacts