DropSafe Safety Needle LD 6069

GUDID 15907996099969

The Dropsafe® Safety Needle is used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.

HTL STREFA S A

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: 15907996099969
• NIH Device Record Key: 88117cb2-aa6a-4ad6-9b58-2b0427fc783b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DropSafe Safety Needle LD
• Version Model Number: 23G x 1"
• Catalog Number: 6069
• Company DUNS: 422528088
• Company Name: HTL STREFA S A
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +484227000010
• Email: info@htl-strefa.com
• Phone: +484227000010
• Email: info@htl-strefa.com
• Phone: +484227000010
• Email: info@htl-strefa.com
• Phone: +484227000010
• Email: info@htl-strefa.com
• Phone: +484227000010
• Email: info@htl-strefa.com
• Phone: +484227000010
• Email: info@htl-strefa.com
• Phone: +484227000010
• Email: info@htl-strefa.com
• Phone: +484227000010
• Email: info@htl-strefa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05907996099962 [Primary]
GS1	15907996099969 [Package]; Contains: 05907996099962; Package: shelf box [100 Units]; In Commercial Distribution
GS1	25907996099966 [Package]; Package: shipper box [8 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123684

FDA Product Code

• FMF: Syringe, Piston

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: 2021-09-14
• Device Publish Date: 2021-09-06

On-Brand Devices [DropSafe Safety Needle LD]

• 15907996099969: The Dropsafe® Safety Needle is used for general purpose injection and aspiration of fluids from
• 05907996099955: The Dropsafe® Safety Needle is used for general purpose injection and aspiration of fluids from