FDA.reportPublic FDA data

8F Base Camp System 2.0 90cm

Primary DI
00853799007930
Brand
8F Base Camp System 2.0 90cm
Company
ROUTE 92 MEDICAL
Model
Gen 2.0
Catalog number
5001-2-90B
Device description
8F Base Camp System 2.0 90cm
Published
2026-07-08
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DQYCatheter, Percutaneous
QJPCatheter, Percutaneous, Neurovasculature

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQYCatheter, PercutaneousCardiovascular2
QJPCatheter, Percutaneous, NeurovasculatureCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K240529000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K2405290008F Modified Sheath SystemRoute 92 Medical, Inc.2024-10-02QJP

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00853799007930PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00853799007930008537990079308537990079300853799007930

GMDN Terms#

Term, Definition table
TermDefinition
Vascular microcatheterA sterile, small-diameter, single-lumen, flexible tube designed for the controlled infusion of fluids (e.g., thrombolytics, diagnostic contrast media) into superselective small vessels (including intracranial, peripheral, or occluded coronary vasculature) for angiography/treatment, and typically also for the delivery of devices (e.g., embolization implants, guidewires) into tortuous vessels or across tight lesions. It may include an ultrasound transducer, a thermal sensor, and a hole for guidewire placement located at the distal tip. It is not a guide-catheter (i.e., is not intended to deliver other catheters or therapeutic leads directly through its lumen). This is a single-use device.

Contacts#

Phone, Email table
PhoneEmail
650-350-9416Customerservice@r92m.com

Regulatory Flags#

DUNS number
067429673
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
false
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
008537990077018F Base Camp system 2.0 80cmGen 2.05001-2-80B2024-10-14
008537990077188F Base Camp system 2.0 80cmGen 2.05001-2-80B2024-10-14
008537990077258F Base Camp system 2.0 90cmGen 2.05001-2-90B2024-10-14
008537990077328F Base Camp system 2.0 90cmGen 2.05001-2-90B2024-10-14
00853799007749FreeClimb 88 catheter, 125cmGen 12024-07-01
00853799007756FreeClimb 88 catheter, 132cmGen 12024-07-01
00853799007763FreeClimb 88 catheter, 125cm with Tenzing 8Gen 17001-88-1252024-07-01
00853799007770FreeClimb 88 catheter, 132cm with Tenzing 8Gen 17001-88-1322024-07-01
00853799007442070 Access SystemGen 1REF 10042024-05-17
00853799007459070 CatheterGen 12024-05-17
00853799007077088 x 125 cm Full Length CatheterGen 12024-05-16
00853799007145088 x 125 cm Full Length Access SystemGen 1REF 40042024-05-16
008537990074118F Base Camp Sheath SystemGen 1.550012024-05-16
00853799007541Tenzing 7 Delivery CatheterGen 12024-05-16
00853799007626FreeClimb 54 x 148 cm CatheterGen 12023-10-16
00853799007633FreeClimb 54 x 125 cm CatheterGen 12023-10-16
00853799007619Tenzing 5 delivery catheterGen 12023-10-16
00853799007640FreeClimb 54 x 148 cm Access SystemGen 1REF 60022024-05-16
00853799007657FreeClimb 54 x 125 cm Access SystemGen 1REF 60042024-05-16
00853799007060088 x 132 cm Full Length CatheterGen 12022-06-22

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Primary DI, Brand, Company table
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10841156111878TURNPIKETELEFLEX INCORPORATEDDQY2025-09-09
00195451000836Shockwave CS Guide CatheterShockwave Medical, Inc.DQY2025-06-02
10801902217773ARROWTELEFLEX INCORPORATEDDQY2024-04-08
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00389701012896R2P NAVICROSSTERUMO MEDICAL CORPORATIONDQY2024-01-11
00389701012902R2P NAVICROSSTERUMO MEDICAL CORPORATIONDQY2024-01-11
10801902215502ARROWTELEFLEX INCORPORATEDDQY2023-07-10
10801902215267ARROWTELEFLEX INCORPORATEDDQY2023-07-07