FDA.report

N/A

Primary DI
00614138122017
Brand
N/A
Company
TETRA MEDICAL SUPPLY CORP.
Model
9800Y3
Catalog number
9800Y3
Device description
EFO 3/4 INSOLE F 8-9.5 & M 8-8.5
Published
2022-08-04
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
false

Related Records

Contact Domains

Product Codes

CodeName
KNPOrthosis, Corrective Shoe

Product Code Classifications

CodeDeviceSpecialtyClass
KNPOrthosis, Corrective ShoePhysical Medicine1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00614138122017PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00614138122017006141381220176141381220170614138122017

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
18006214041sales@tetramed.com

Regulatory Flags

DUNS number
047580212
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
false
Manufacturing date on label
false
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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00614138105157N/A1214141214142022-08-19
00614138105164N/A1214151214152022-08-19
00614138106147N/A1213021213022022-08-19
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00614138113435N/A2149-022149-022022-08-19
00614138113442N/A2149-032149-032022-08-19
00614138113459N/A2149-042149-042022-08-19
00614138113466N/A2149-062149-062022-08-19

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