Primary Device ID | 00634624031500 |
NIH Device Record Key | 7747d307-18cf-4c92-91bf-9437af3950e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Q2® Needleless injection site |
Version Model Number | 3150 |
Catalog Number | 3150 |
Company DUNS | 041810693 |
Company Name | QUEST MEDICAL INC |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00634624031500 [Primary] |
GS1 | 10634624031507 [Package] Package: Carton [50 Units] |
GS1 | 20634624031504 [Package] Contains: 10634624031507 Package: Shipper [4 Units] |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-09-23 |
Device Publish Date | 2017-03-09 |
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