Primary Device ID | 10383790002605 |
NIH Device Record Key | 5faf250f-28ae-408b-ab67-8e7d0a90a7bb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NIPRO SafeTouch™ Safety Scalp Vein Set |
Version Model Number | SPR+23G19 |
Company DUNS | 797372554 |
Company Name | NIPRO MEDICAL CORPORATION |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1 (908) 393-7030 |
info@nipromed.com | |
Phone | +1 (908) 393-7030 |
info@nipromed.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 Issuing Agency | Device ID |
---|---|
GS1 | 00383790002608 [Primary] |
GS1 | 10383790002605 [Package] Contains: 00383790002608 Package: [50 Units] In Commercial Distribution |
GS1 | 40383790002606 [Package] Package: [10 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 | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-16 |
40383790002613 | SPR+25G19 |
10383790002605 | SPR+23G19 |
10383790002599 | SPR+21G19 |
40383790002583 | SPR+19G19 |