IMPEDE Embolization Plug

Primary DI
B054IMP071
Brand
IMPEDE Embolization Plug
Company
Shape Memory Medical Inc.
Model
IMP-07
Catalog number
IMP-07
Device description
IMPEDE Embolization Plug 7mm
Published
2019-10-31
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
KRDDevice, Vascular, For Promoting Embolization

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KRDDevice, Vascular, For Promoting EmbolizationCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K181051000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K181051000IMPEDE Embolization Plug, 5mm, IMPEDE Embolization Plug, 7mm, IMPEDE Embolization Plug, 10mmShape Memory Medical2018-06-22KRD

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B054IMP071PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Vascular occluder, single-useA device intended to be used to mechanically stop or interrupt the flow of blood in veins or arteries temporarily during vascular surgery and emergency trauma surgery. It is typically designed with a ring having a small portion left open so that it can be slipped over the blood vessel to be occluded, or it can have semicircular pivoted arms that can be opened and placed over the vessel with a latch to lock the arms once in place. The inner surface of this ring is lined with a soft-plastic balloon, or pair of balloons, inflated via a connecting tube using a standard syringe. This device facilitates occlusion with minimal trauma to the wall of the blood vessel. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
025984823
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810041650009IMPEDE Embolization PlugIMP-05IMP-052020-04-02
00810041650016IMPEDE Embolization PlugIMP-07IMP-072020-04-02
00810041650023IMPEDE Embolization PlugIMP-10IMP-102020-04-02
00810041650030IMPEDE-FX Embolization PlugIMP-FX-06IMP-FX-062020-04-02
00810041650047IMPEDE-FX Embolization PlugIMP-FX-08IMP-FX-082020-04-02
00810041650054IMPEDE-FX Embolization PlugIMP-FX-12IMP-FX-122020-04-02
B054IMP051IMPEDE Embolization PlugIMP-05IMP-052019-10-31
B054IMP101IMPEDE Embolization PlugIMP-10IMP-102019-10-31
B054IMPFX061IMPEDE-FX Embolization PlugIMP-FX-06IMP-FX-062019-10-31
B054IMPFX081IMPEDE-FX Embolization PlugIMP-FX-08IMP-FX-082019-10-31
B054IMPFX121IMPEDE-FX Embolization PlugIMP-FX-12IMP-FX-122019-10-31

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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10857798005109Nitinol Enhanced DeviceEmbolization Inc.KRD2026-02-12
10857798005123Nitinol Enhanced DeviceEmbolization Inc.KRD2026-02-12
10857798005130Nitinol Enhanced DeviceEmbolization Inc.KRD2026-02-12
10857798005147Nitinol Enhanced DeviceEmbolization Inc.KRD2026-02-12
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07613327578744Target TetraStryker CorporationKRD2022-12-19
07613327580099Target TetraStryker CorporationKRD2022-12-19
10841156106591GEL-BEADTELEFLEX INCORPORATEDKRD2020-04-23
10841156106614GEL-BEADTELEFLEX INCORPORATEDKRD2020-04-23
10841156106621GEL-BEADTELEFLEX INCORPORATEDKRD2020-04-23
10841156106638GEL-BEADTELEFLEX INCORPORATEDKRD2020-04-23
07613327466386TARGETStryker CorporationKRD2019-09-05
07613327466416TARGETStryker CorporationKRD2019-09-05
07613327466423TARGETStryker CorporationKRD2019-09-05
10841156100001OPTISPHERETELEFLEX INCORPORATEDKRD2018-03-27
10841156100018OPTISPHERETELEFLEX INCORPORATEDKRD2018-03-27
10841156100025OPTISPHERETELEFLEX INCORPORATEDKRD2018-03-27
10841156100032OPTISPHERETELEFLEX INCORPORATEDKRD2018-03-27