LIN LEAD 18G

GUDID 03665134000301

Needle guide compatible with the linear 2D ultrasound probe. It is made of two parts. One part is fixed on the ultrasound probe. The other removable part is perforated and inserted in the first part to guide the needle. The device is designed to guide needles with a diameter from 17G to 20G. The guides are reusable after appropriate procedure. They are not delivered in sterile condition

KOELIS

Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable

• Primary Device ID: 03665134000301
• NIH Device Record Key: b40df982-a3ad-44dd-9706-4a5108ca0b62
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIN LEAD 18G
• Version Model Number: KRNG.LN.18
• Company DUNS: 290318455
• Company Name: KOELIS
• Device Count: 5
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com
• Phone: +33(0)458176810
• Email: qra@koelis.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03665134000196 [Unit of Use]
GS1	03665134000301 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171040

FDA Product Code

• ITX: Transducer, Ultrasonic, Diagnostic

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

[03665134000301]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-13
• Device Publish Date: 2023-04-05

Devices Manufactured by KOELIS

• 03665134000929 - MrDraw: 2023-10-10 A system based on the PROMAP – 3D Prostate Suite range intended to define prostate contour and targets the region of interest
• 03665134000509 - 3D End-Fire Endocavity Probe: 2023-04-13 Invasive 2D/3D endocavity probe (linear) to be used with TRINITY ultrasound system KURO-3000-X This probe is used for 2D exam, 3
• 03665134000516 - 3D Side-Fire Endocavity Probe: 2023-04-13 Invasive 2D/3D endocavity probe (linear) to be used with TRINITY ultrasound system KURO-3000-X This probe is used for 2D exam, 3
• 03665134000523 - 2D Abdominal Probe: 2023-04-13 Surface 2D probe (Convex) to be used with TRINITY ultrasound system KURO-3000-X This probe is used for 2D exam for Abdominal, Gy
• 03665134000530 - 2D Linear Probe: 2023-04-13 Surface 2D probe (linear) to be used with TRINITY ultrasound system KURO-3000-X This probe is used for 2D exam for Abdominal, Gy
• 03665134000189 - CON LEAD 14G: 2023-04-13 Needle guide compatible with the abdominal 2D ultrasound probe. It is made of two parts. One part is fixed on the ultrasound pro
• 03665134000301 - LIN LEAD 18G: 2023-04-13Needle guide compatible with the linear 2D ultrasound probe. It is made of two parts. One part is fixed on the ultrasound probe. The other removable part is perforated and inserted in the first part to guide the needle. The device is designed to guide needles with a diameter from 17G to 20G. The guides are reusable after appropriate procedure. They are not delivered in sterile condition
• 03665134000301 - LIN LEAD 18G: 2023-04-13 Needle guide compatible with the linear 2D ultrasound probe. It is made of two parts. One part is fixed on the ultrasound probe.
• 03665134000318 - LIN LEAD 14G: 2023-04-13 Needle guide compatible with the linear 2D ultrasound probe. It is made of two parts. One part is fixed on the ultrasound probe.