FDA.report

MEDI

Primary DI
00636257040904
Brand
MEDI
Company
MEDI MANUFACTURING, INC.
Model
FS10640
Device description
FOOT SOLUTIONS PF PRO 40
Published
2022-10-31
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
true

Related Records

Product Codes

CodeName
IQIORTHOSIS, LIMB BRACE

Product Code Classifications

CodeDeviceSpecialtyClass
IQIOrthosis, Limb BracePhysical Medicine1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00636257040904PrimaryGS10

GMDN Terms

TermDefinition
Orthotic insole, prefabricated, non-antimicrobialA prefabricated shoe insert typically available for use by a layperson intended to provide supplemental support for the arch and/or heel of the foot; it does not include an antimicrobial agent(s). This is a reusable device.

Sterilization Methods

Method

Contacts

PhoneEmail
+1(800)633-6334info@mediusa.com

Regulatory Flags

DUNS number
960754430
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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00636257211304MEDIKCOR2CM32026-03-17
00636257211311MEDIKCOR2CM42026-03-17
00636257211328MEDIKCOR2LT12026-03-17
00636257211335MEDIKCOR2LT22026-03-17
00636257211342MEDIKCOR2LT32026-03-17
00636257211359MEDIKCOR2LT42026-03-17
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00636257211373MEDIKCOR2MC22026-03-17
00636257211380MEDIKCOR2MC32026-03-17
00636257211397MEDIKCOR2MC42026-03-17
00636257211403MEDIKBST2DR12026-03-17
00636257211410MEDIKBST2DR22026-03-17
00636257211427MEDIKBST2DR32026-03-17
00636257211434MEDIKBST2DR42026-03-17
00636257211441MEDIKBST2FG12026-03-17
00636257211458MEDIKBST2FG22026-03-17
00636257211465MEDIKBST2FG32026-03-17
00636257211472MEDIKBST2FG42026-03-17

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