Primary Device ID | 44900719326047 |
NIH Device Record Key | f52814e3-491d-474a-86cb-bf82917465b3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Phoenix |
Version Model Number | TUFW20G350 |
Company DUNS | 701082349 |
Company Name | DR.JAPAN CO., LTD. |
Device Count | 100 |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Length | 3.5 Inch |
Needle Gauge | 20 Gauge |
Length | 3.5 Inch |
Needle Gauge | 20 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04900719326049 [Unit of Use] |
GS1 | 44900719326047 [Primary] |
BSP | Needle, Conduction, Anesthetic (W/Wo Introducer) |
Steralize Prior To Use | true |
Device Is Sterile | false |
[44900719326047]
Ethylene Oxide
[44900719326047]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-24 |