FDA.reportPublic FDA data

SENDERO

Primary DI
00850008222085
Brand
SENDERO
Company
OKAMI MEDICAL, INC.
Model
SENDERO-MAX55-110MP
Device description
Delivery Catheter
Published
2025-04-24
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DQYCatheter, Percutaneous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQYCatheter, PercutaneousCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K242644000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K242644000SENDERO MAX Delivery CatheterOkami Medical, Inc.2024-12-20DQY

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850008222085PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850008222085008500082220858500082220850850008222085

GMDN Terms#

Term, Definition table
TermDefinition
Vascular guide-catheter, single-useA flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended solely for infusion, is not intended to access superselective small vessels, and does not include a transseptal needle. It may include a disposable percutaneous introduction set or shaft visualization electrodes. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
9494469710info@okamimedical.com

Regulatory Flags#

DUNS number
117045423
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850008222092LOBOLOBO-3-LP2026-05-19
00850008222078SENDEROSENDERO-MC29-1302024-04-05
00850008222030LOBOLOBO-72022-06-28
00850008222061LOBOLOBO-92022-06-28
00850008222009LOBOLOBO-HP2020-01-07
00850008222054LOBOLOBO-52021-02-09
00850008222016LOBOLOBO-32020-01-07

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00810024671953SSPC NXT Delivery CatheterCENTERPOINT SYSTEMS LLCDQY2026-06-01
08718481740330Guidion ShortIMDS Operations B.V.DQY2026-06-01
08718481740347FlowGuideIMDS Operations B.V.DQY2026-06-01
07613327623338AXS LiftStryker CorporationDQY2025-03-04
07613327623376AXS LiftStryker CorporationDQY2025-03-04
00763000270346Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-08
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00763000270520Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-08
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00763000270704Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-08
00763000270711Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-08
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00763000270308Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-07
00763000270315Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-07
00763000270322Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-07
00763000270339Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-07
00763000270391Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-07
00763000270407Solitaire™ X-PACKMicro Therapeutics, Inc.DQY2019-11-07