FDA.reportPublic FDA data

Caterpillar

Primary DI
00801741155314
Brand
Caterpillar
Company
CLEARSTREAM TECHNOLOGIES LIMITED
Model
CTP038020U
Catalog number
CTP038020U
Device description
Caterpillar Arterial Embolization Device, 0.038 Inch ID Catheter Compatibility
Published
2020-02-13
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Contact Domains#

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
K191532000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K191532000The Caterpillar and Caterpillar Micro Arterial Embolization DevicesC.R. Bard, Inc.2020-02-04KRD

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00801741155314PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00801741155314008017411553148017411553140801741155314

GMDN Terms#

Term, Definition table
TermDefinition
Non-neurovascular embolization plug, metallicA sterile, non-bioabsorbable, metal device intended to be implanted in a non-neurovascular blood vessel, permanently or long-term, to occlude blood flow typically for treatment of an aneurysm, tumour (e.g., nephroma, hepatoma, uterine fibroids), and/or arteriovenous malformation (AVM). It is in the form of an expandable metal scaffold, which once expanded is intended to induce thrombosis and create a blockage; it is typically supplied with instruments dedicated to implantation. This device is not intended to be used in intracranial arteries or for other neurovascular applications.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)321-4254medical.services@crbard.com

Regulatory Flags#

DUNS number
989214291
Device count
1
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00801741184802Halo One™ Thin-Walled Guiding SheathHLO41018FHHLO41018FH2020-04-27
00801741184819Halo One™ Thin-Walled Guiding SheathHLO41035FHHLO41035FH2020-04-27
00801741184833Halo One™ Thin-Walled Guiding SheathHLO51018FHHLO51018FH2020-04-27
00801741184840Halo One™ Thin-Walled Guiding SheathHLO51035FHHLO51035FH2020-04-27
00801741184864Halo One™ Thin-Walled Guiding SheathHLO61035FHHLO61035FH2020-04-27
00801741223778Halo One Thin-Walled Guiding SheathHLO41018FHKHLO41018FHK2021-12-14
00801741223785Halo One Thin-Walled Guiding SheathHLO41035FHKHLO41035FHK2021-12-14
00801741223815Halo One Thin-Walled Guiding SheathHLO51018FHKHLO51018FHK2021-12-14
00801741223822Halo One Thin-Walled Guiding SheathHLO51035FHKHLO51035FHK2021-12-14
00801741223853Halo One Thin-Walled Guiding SheathHLO61035FHKHLO61035FHK2021-12-14
00801741223907Halo One Thin-Walled Guiding SheathHLO61018FHKHLO61018FHK2021-12-14
00801741184826Halo One™ Thin-Walled Guiding SheathHLO42535HHLO42535H2020-04-27
00801741184857Halo One™ Thin-Walled Guiding SheathHLO52535HHLO52535H2020-04-27
00801741184871Halo One™ Thin-Walled Guiding SheathHLO62535HHLO62535H2020-04-27
00801741223792Halo One Thin-Walled Guiding SheathHLO42518HKHLO42518HK2021-12-14
00801741223808Halo One Thin-Walled Guiding SheathHLO42535HKHLO42535HK2021-12-14
00801741223839Halo One Thin-Walled Guiding SheathHLO52518HKHLO52518HK2021-12-14
00801741223846Halo One Thin-Walled Guiding SheathHLO52535HKHLO52535HK2021-12-14
00801741223860Halo One Thin-Walled Guiding SheathHLO62535HKHLO62535HK2021-12-14
00801741223914Halo One Thin-Walled Guiding SheathHLO62518HKHLO62518HK2021-12-14

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