Guidewire Introducer Needle GWI-1902

GUDID 20813079020336

19ga (1.1mm) x 7 cm

REMINGTON MEDICAL, INC.

Intra-arterial needle

• Primary Device ID: 20813079020336
• NIH Device Record Key: bd83aa67-bacc-42f5-936a-d040a73320e0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guidewire Introducer Needle
• Version Model Number: GWI-1902
• Catalog Number: GWI-1902
• Company DUNS: 788472314
• Company Name: REMINGTON MEDICAL, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com
• Phone: +1(800)989-0057
• Email: Quality@Remmed.com

Device Dimensions

• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge
• Needle Gauge: 19 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813079020332 [Primary]
GS1	10813079020339 [Package]; Contains: 00813079020332; Package: Inner Carton [10 Units]; In Commercial Distribution
GS1	20813079020336 [Package]; Contains: 10813079020339; Package: Shipping Carton [10 Units]; In Commercial Distribution

FDA Product Code

• DWS: INSTRUMENTS, SURGICAL, CARDIOVASCULAR

Sterilization

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

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

[20813079020336]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-10-02
• Device Publish Date: 2020-09-24

On-Brand Devices [Guidewire Introducer Needle]

• 20813079020336: 19ga (1.1mm) x 7 cm
• 20813079020305: 18ga (1.3mm) x 7cm