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 |
Phone | +484227000010 |
info@htl-strefa.com | |
Phone | +484227000010 |
info@htl-strefa.com | |
Phone | +484227000010 |
info@htl-strefa.com | |
Phone | +484227000010 |
info@htl-strefa.com | |
Phone | +484227000010 |
info@htl-strefa.com | |
Phone | +484227000010 |
info@htl-strefa.com | |
Phone | +484227000010 |
info@htl-strefa.com | |
Phone | +484227000010 |
info@htl-strefa.com |
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 |
FMF | Syringe, Piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-14 |
Device Publish Date | 2021-09-06 |
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 |