Primary Device ID | 10850017259031 |
NIH Device Record Key | 548b95bb-067e-47f2-9a23-709346d5a2dd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Luther Needlesafe Products |
Version Model Number | 22150001 |
Catalog Number | 22150001 |
Company DUNS | 117440613 |
Company Name | Luther Needlesafe Products, LLC |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850017259034 [Primary] |
GS1 | 10850017259031 [Package] Contains: 00850017259034 Package: Inner Box [50 Units] In Commercial Distribution |
FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-09 |
Device Publish Date | 2023-05-01 |
00850017259058 | Mini-Midline Extended Dwell Peripheral Catheter - 24Ga, 1.25” |
10850017259048 | Mini-Midline Extended Dwell Peripheral Catheter - 22Ga, 1.75” |
10850017259031 | Mini-Midline Extended Dwell Peripheral Catheter - 22Ga, 1.50” |
10850017259024 | Mini-Midline Extended Dwell Peripheral Catheter - 20Ga, 1.75” |
10850017259017 | Mini-Midline Extended Dwell Peripheral Catheter - 20Ga, 1.50” |
10850017259000 | Mini-Midline Extended Dwell Peripheral Catheter - 18Ga, 1.75” |