Primary Device ID | M991TH021002 |
NIH Device Record Key | 714de9ea-3d5b-43e5-b9ba-19cdcf8f3105 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tidal High-Flow Non-coring Needle |
Version Model Number | Tidal-HF |
Catalog Number | TH02100 |
Company DUNS | 013861471 |
Company Name | NORFOLK MEDICAL |
Device Count | 1 |
DM Exempt | true |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(847)674-7075 |
npheil@norfolkmedical.com |
Needle Gauge | 16 Gauge |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M991TH021001 [Primary] |
HIBCC | M991TH021002 [Package] Contains: M991TH021001 Package: Box [10 Units] In Commercial Distribution |
FMI | Needle, hypodermic, single lumen |
Steralize Prior To Use | true |
Device Is Sterile | true |
[M991TH021002]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2015-10-06 |
M991TH023002 | 16G x 1-1/4" Tidal High-Flow Non-coring Needle |
M991TH022002 | 16G x 1" Tidal High-Flow Non-coring Needle |
M991TH021002 | 16G x 3/4" Tidal High-Flow Non-coring Needle |
M991TH013002 | 18G x 1-1/4" Tidal High-Flow Non-coring Needle |
M991TH012002 | 18G x 1" Tidal High-Flow Non-coring Needle |
M991TH011002 | 18G x 3/4" Tidal High-Flow Non-coring Needle |