Primary Device ID | 10383790006245 |
NIH Device Record Key | 31c7f92d-17b9-4616-9c33-2e581613239a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NIPRO AQUALiner™ |
Version Model Number | ALS+38180SS |
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 |
Outer Diameter | 0.038 Inch |
Outer Diameter | 0.038 Inch |
Length | 180 Centimeter |
Outer Diameter | 0.038 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00383790006248 [Primary] |
GS1 | 10383790006245 [Package] Contains: 00383790006248 Package: [5 Units] In Commercial Distribution |
GS1 | 40383790006246 [Package] Package: [10 Units] In Commercial Distribution |
DQX | WIRE, GUIDE, CATHETER |
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 |
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