FDA UDI Not in Commercial Distribution 🇺🇸 United States

LF900

DI: 08809315677202 · Model: LF90200-ROL · DAESUNG MAREF CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LF900
Primary DI
08809315677202
Version / Model
LF90200-ROL
Company Name
DAESUNG MAREF CO.,LTD.
Labeler DUNS
688817949
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-14
Public Version
1
Public Version Date
2021-12-22
Public Version Status
New
Public Device Record Key
d93136e8-6e67-498a-9488-34456578185a
Distribution End Date
2021-12-14

Device Description

Main device 1ea, OVERLAPPING LEG SLEEVE Large(L401) 2ea, Double Hose 1ea, Recovery Bag 1ea [One set box]

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IRP Massager, Powered Inflatable Tube

GMDN Terms

Code Name
10969 Intermittent venous compression system

Identifiers

Type ID
Primary 08809315677202

Premarket Submissions

Submission Number Supplement Number
K203019 000