EZ FLO NEZ21200

GUDID 20850017403134

HYPODERMIC NEEDLE 21G X 2"

AIR-TITE PRODUCTS COMPANY, INC.

Hypodermic needle, single-use Hypodermic needle, single-use Hypodermic needle, single-use Hypodermic needle, single-use Hypodermic needle, single-use Hypodermic needle, single-use Hypodermic needle, single-use Hypodermic needle, single-use Hypodermic needle, single-use

• Primary Device ID: 20850017403134
• NIH Device Record Key: 2a202eef-6149-4351-9b79-a910262a8be2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EZ FLO
• Version Model Number: NEZ21200
• Catalog Number: NEZ21200
• Company DUNS: 002385425
• Company Name: AIR-TITE PRODUCTS COMPANY, INC.
• Device Count: 100
• 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: true
• 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: (757) 340-2501
• Email: atinfo@air-tite.com
• Phone: (757) 340-2501
• Email: atinfo@air-tite.com
• Phone: (757) 340-2501
• Email: atinfo@air-tite.com
• Phone: (757) 340-2501
• Email: atinfo@air-tite.com
• Phone: (757) 340-2501
• Email: atinfo@air-tite.com
• Phone: (757) 340-2501
• Email: atinfo@air-tite.com
• Phone: (757) 340-2501
• Email: atinfo@air-tite.com
• Phone: (757) 340-2501
• Email: atinfo@air-tite.com
• Phone: (757) 340-2501
• Email: atinfo@air-tite.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850017403130 [Unit of Use]
GS1	10850017403137 [Primary]
GS1	20850017403134 [Package]; Contains: 10850017403137; Package: CASE [20 Units]; In Commercial Distribution
GS1	30850017403131 [Package]; Package: MASTER CASE [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112057

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: 2020-04-23
• Device Publish Date: 2020-04-15

On-Brand Devices [EZ FLO]

• 20850017403325: HYPODERMIC NEEDLE 30G X 1"
• 20850017403318: HYPODERMIC NEEDLE 30G X 1/2"
• 20850017403301: HYPODERMIC NEEDLE 27G X 2"
• 20850017403295: HYPODERMIC NEEDLE 27G X 1-1/4"
• 20850017403288: HYPODERMIC NEEDLE 27G X 1-1/2"
• 20850017403271: HYPODERMIC NEEDLE 27G X 1"
• 20850017403264: HYPODERMIC NEEDLE 25G X 2"
• 20850017403257: HYPODERMIC NEEDLE 25G X 1-1/2"
• 20850017403240: HYPODERMIC NEEDLE 25G X 1"
• 20850017403233: HYPODERMIC NEEDLE 25G X 5/8"
• 20850017403226: HYPODERMIC NEEDLE 23G X 1-1/2"
• 20850017403219: HYPODERMIC NEEDLE 23G X 1"
• 20850017403202: HYPODERMIC NEEDLE 23G X 3/4"
• 20850017403196: HYPODERMIC NEEDLE 22G X 4"
• 20850017403189: HYPODERMIC NEEDLE 22G X 3"
• 20850017403172: HYPODERMIC NEEDLE 22G X 1-1/2"
• 20850017403165: HYPODERMIC NEEDLE 22G X 2"
• 20850017403158: HYPODERMIC NEEDLE 22G X 1"
• 20850017403141: HYPODERMIC NEEDLE 22G X 3/4"
• 20850017403134: HYPODERMIC NEEDLE 21G X 2"
• 20850017403127: HYPODERMIC NEEDLE 21G X 1-1/2"
• 20850017403110: HYPODERMIC NEEDLE 21G X 1"
• 20850017403103: HYPODERMIC NEEDLE 20G X 1-1/2"
• 20850017403097: HYPODERMIC NEEDLE 20G X 1"
• 20850017403080: HYPODERMIC NEEDLE 19G X 1-1/2"
• 20850017403073: HYPODERMIC NEEDLE 19G X 1"
• 20850017403066: HYPODERMIC NEEDLE 18G X 2"
• 20850017403059: HYPODERMIC NEEDLE 18G X 1-1/2"
• 20850017403042: HYPODERMIC NEEDLE 18G X 1"
• 20850017403035: HYPODERMIC NEEDLE 17G X 2"
• 20850017403028: HYPODERMIC NEEDLE 16G X 1-1/2"
• 20850017403011: HYPODERMIC NEEDLE 16G X 1"
• 20850017403004: HYPODERMIC NEEDLE 15G X 1-1/2"
• 20850017403363: HYPODERMIC NEEDLE 18G X 3/4"