Primary Device ID | 20634624095469 |
NIH Device Record Key | 0d95a32d-4248-4fba-aae8-a7fd702d9770 |
Commercial Distribution Discontinuation | 2019-02-13 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | 18 in (46 cm) Q2 Extension set w/ standard bore tubing |
Version Model Number | 9546 |
Catalog Number | 9546 |
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 | 00634624095465 [Primary] |
GS1 | 20634624095469 [Package] Contains: 00634624095465 Package: Shipper [50 Units] Discontinued: 2019-02-13 Not in Commercial Distribution |
FPK | Tubing, Fluid Delivery |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-06-11 |
Device Publish Date | 2016-07-29 |
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