Eclipse DermaFlex MicroCannula DF25G50MM23G

GUDID 10853602008489

DermaFlex Microcannula 25G/50mm + 23G/25mm Pilot

ECLIPSE

Hypodermic needle, single-use

• Primary Device ID: 10853602008489
• NIH Device Record Key: ec47e126-d00b-4b64-8c9e-f8d3dacae9a0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Eclipse DermaFlex MicroCannula
• Version Model Number: DF25G50MM23G
• Catalog Number: DF25G50MM23G
• Company DUNS: 969752364
• Company Name: ECLIPSE
• Device Count: 1
• 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: 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: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com
• Phone: 8007596876
• Email: sales@eclipsemed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00853602008482 [Primary]
GS1	10853602008489 [Package]; Contains: 00853602008482; Package: Box [25 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K200017

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-31
• Device Publish Date: 2021-03-23

On-Brand Devices [Eclipse DermaFlex MicroCannula]

• 10853602008526: DermaFlex Microcannula 30G/25mm + 27G/25mm Pilot
• 10853602008519: DermaFlex Microcannula 27G/50mm + 26G/25mm Pilot
• 10853602008502: DermaFlex Microcannula 27G/38mm + 26G/25mm Pilot
• 10853602008496: DermaFlex Microcannula 27G/25mm + 26G/25mm Pilot
• 10853602008489: DermaFlex Microcannula 25G/50mm + 23G/25mm Pilot
• 10853602008472: DermaFlex Microcannula 25G/40mm + 23G/25mm Pilot
• 00853602008468: DermaFlex Microcannula 22G/70mm + 21G/25mm Pilot
• 10853602008458: DermaFlex Microcannula 22G/60mm + 21G/25mm