FDA UDI In Commercial Distribution 🇺🇸 United States

Lumex

DI: M368LF1030S1 · Model: LF1030S · GF HEALTH PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lumex
Primary DI
M368LF1030S1
Version / Model
LF1030S
Catalog Number
LF1030S
Company Name
GF HEALTH PRODUCTS, INC.
Labeler DUNS
132016168
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-14
Public Version
2
Public Version Date
2021-11-23
Public Version Status
Update
Public Device Record Key
1b4c0e7d-40ab-4ea3-9b39-00c40adbc546

Device Description

PATIENT LIFT HYDRAULIC BLUE, LARGE SLING

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
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
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 M368LF1030S1

Customer Contacts

Phone
770-368-4700