DropSafe Sicura 02094000210250

GUDID 20812383030918

PASSIVE SAFETY NEEDLE DROPSAFE SICURA G21x25mm 50p

PIKDARE SPA

Hypodermic needle, single-use

• Primary Device ID: 20812383030918
• NIH Device Record Key: 01b69aa6-ce0f-4183-a0ac-c541e4d2e7f8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DropSafe Sicura
• Version Model Number: 02094000210250
• Catalog Number: 02094000210250
• Company DUNS: 437816603
• Company Name: PIKDARE SPA
• Device Count: 50
• 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: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com
• Phone: 1-877-660-1900
• Email: info@htl-strefa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812383030914 [Primary]
GS1	10812383030911 [Unit of Use]
GS1	20812383030918 [Package]; Contains: 00812383030914; Package: BOX [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223353

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-06-05
• Device Publish Date: 2022-12-23

On-Brand Devices [DropSafe Sicura]

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• 20812383030963: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G27x13mm 50p
• 20812383030956: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G25x16mm 50p
• 20812383030949: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G25x25mm 50p
• 20812383030932: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G23x25mm 50p
• 20812383030925: PASSIVE SAFETY NEEDLE G22x25mm 50p
• 20812383030918: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G21x25mm 50p
• 20812383030901: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G18x25mm 50p
• 20812383031014: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G30X13 5P
• 20812383031007: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G27X13 5P
• 20812383030994: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G25X16mm
• 20812383030987: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G25X25mm 5 p
• 20812383030888: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G23X25 5 P
• 20812383030871: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G22X25 5 P
• 20812383030864: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G21X25 5P
• 20812383030857: PASSIVE SAFETY NEEDLE DROPSAFE SICURA G18X25 5P