FDA UDI In Commercial Distribution 🇺🇸 United States

LUMEX

DI: M368FMC1161 · Model: FMC116 · GF HEALTH PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
LUMEX
Primary DI
M368FMC1161
Version / Model
FMC116
Company Name
GF HEALTH PRODUCTS, INC.
Labeler DUNS
132016168
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-01
Public Version
1
Public Version Date
2023-12-11
Public Version Status
New
Public Device Record Key
8c77b897-7abd-4d56-9ad8-065724735665

Device Description

FULL BODY SLING MESH/CMD X-LGE

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
FNG Lift, Patient, Ac-Powered

GMDN Terms

Code Name
40535 Solid-seat mobile patient lifting system seat

Identifiers

Type ID
Primary M368FMC1161

Customer Contacts

Phone
7703684700