Primary Device ID | 40383790002477 |
NIH Device Record Key | 203dd39b-1204-4423-bcf4-d026be1c3f3a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NIPRO SCALP VEIN SET |
Version Model Number | PR+19G19 |
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 | 00383790002479 [Primary] |
GS1 | 10383790002476 [Package] Contains: 00383790002479 Package: [50 Units] In Commercial Distribution |
GS1 | 40383790002477 [Package] Contains: 10383790002476 Package: [20 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 |
40383790002552 | PR+27G19 |
10383790002537 | PR+25G19 |
10383790002513 | PR+23G19 |
40383790002507 | PR+22G19 |
40383790002491 | PR+21G19 |
40383790002477 | PR+19G19 |
10383790002469 | PR+18G19 |