INTRAgen Tip

Primary DI
08800020101211
Brand
INTRAgen Tip
Company
Jeisys Medical Inc.
Model
KT-15
Device description
INTRAgen Tip (KT-15)
Published
2022-03-29
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
GEIElectrosurgical, Cutting & Coagulation & Accessories
OUHSkin Resurfacing Rf Applicator

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2
OUHSkin Resurfacing Rf ApplicatorGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K142833000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K142833000INTRAGenJeisys Medical, Inc.2015-06-04OUH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08800020111821PackageGS110In Commercial Distribution
18800020101218PackageGS110In Commercial Distribution
08800020101211PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08800020111821088000201118218800020111821
1880002010121818800020101218
08800020101211088000201012118800020101211

GMDN Terms#

Term, Definition table
TermDefinition
Radio-frequency skin contouring system applicator tipA removable endpiece that is attached to a radio-frequency (RF) skin contouring system applicator (handpiece), used to regulate the delivery of RF energy to the patient during treatment. As a procedural safety measure, the device may permit the transfer of energy only when a correct surface contact is established. It may also be used to cool the skin and monitor its temperature to protect the epidermis during treatment. This is a single-use device.

Regulatory Flags#

DUNS number
690275362
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08800020110688INTRAGen HandpieceINTRAGen Handpiece2026-07-29
08800020100153LIPOcelLIPOcel2026-07-21
08800020100481POTENZA TipCP-21 TIP2026-07-21
08800020101754POTENZA HandpieceAC Handpiece2026-07-21
08800020101761POTENZA HandpieceS Handpiece2026-07-21
08800020101778POTENZA HandpieceMotor Handpiece2026-07-21
08800020101891FootswitchLIPOcel_Foot Switch2026-07-21
08800020109088LIPOcel CartridgeL13 Cartridge2026-07-21
08800020109439TRI-BEAM ARMTRI-BEAM Articulated Arm 022026-07-21
08800020110541INTRAcel PremiumINTRAcel Premium Fractional RF Micro Needle (FRM) 2026-07-21
08800020111845P-NAIN SYSTEMP-NAIN SYSTEM2026-07-21
08800020111852HILTHERAHILTHERA 4.02026-07-21
08800020105028INTRAgen TipKT-072016-10-31
08800020100276INTRAcel TipINTRAcel Tip 10102026-07-16
08800020100283INTRAcel TipINTRAcel Tip 32026-07-16
08800020100306INTRAcel TipINTRAcel Tip 10122026-07-16
08800020100313INTRAcel TipINTRAcel Tip 10132026-07-16
08800020100320INTRAcel TipINTRAcel Tip 20112026-07-16
08800020100337INTRAcel TipN16 Tip2026-07-16
08800020104984DENSITY TipClassic-B Tip2026-07-16

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00841019123713KirwanKIRWAN SURGICAL PRODUCTS LLCGEI2026-08-19
00841019123720KirwanKIRWAN SURGICAL PRODUCTS LLCGEI2026-08-19
00841019123737KirwanKIRWAN SURGICAL PRODUCTS LLCGEI2026-08-19
00841019123744KirwanKIRWAN SURGICAL PRODUCTS LLCGEI2026-08-19
00841019124154KirwanKIRWAN SURGICAL PRODUCTS LLCGEI2026-08-19
00190776414733MillenniumAvalign Technologies, Inc.GEI2026-08-18
00190776415310MillenniumAvalign Technologies, Inc.GEI2026-08-18
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