Primary Device ID | 20812383030871 |
NIH Device Record Key | 4671e984-3e2b-4d48-9202-5b75114b7c40 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DropSafe Sicura |
Version Model Number | 02099940220250 |
Catalog Number | 02099940220250 |
Company DUNS | 437816603 |
Company Name | PIKDARE SPA |
Device Count | 5 |
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 |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com | |
Phone | 1-877-660-1900 |
info@htl-strefa.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812383030877 [Primary] |
GS1 | 10812383030928 [Unit of Use] |
GS1 | 20812383030871 [Package] Contains: 00812383030877 Package: BOX [40 Units] In Commercial Distribution |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-24 |
Device Publish Date | 2023-07-16 |
20812383030970 | PASSIVE SAFETY NEEDLE DROPSAFE SICURA G30x13mm |
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 |