FDA UDI In Commercial Distribution 🇺🇸 United States

LF400

DI: 08809802640320 · Model: LF40100-OHW · DAESUNG MAREF CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
LF400
Primary DI
08809802640320
Version / Model
LF40100-OHW
Company Name
DAESUNG MAREF CO.,LTD.
Labeler DUNS
688817949
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-15
Public Version
1
Public Version Date
2021-12-23
Public Version Status
New
Public Device Record Key
555e4d64-535d-41f9-bb52-0b3f4b67bc6b

Device Description

Main device 1ea, OVERLAPPING HALF-LEG SLEEVE Medium Wide(MW403) 2ea, Single Hose 2ea [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
Package 18809802640327
Primary 08809802640320

Premarket Submissions

Submission Number Supplement Number
K150033 000