FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10197344026166 · Model: MDSAMPUTEEXL · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10197344026166
Version / Model
MDSAMPUTEEXL
Catalog Number
MDSAMPUTEEXL
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-09
Public Version
1
Public Version Date
2023-11-17
Public Version Status
New
Public Device Record Key
a41e45f2-8e7f-4a54-bb4d-ae6c0b6e187d

Device Description

SLING, AMPUTEE, REUSE, XLRG, EA

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
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
FSA Lift, patient, non-ac-powered

GMDN Terms

Code Name
37480 General-purpose patient lifting system sling/harness

Identifiers

Type ID
Primary 10197344026166

Customer Contacts