Multi-Sampling Connector 4R5129

GUDID 24086000101268

Semi-Assembled Multi-Sample Access Device.

Fresenius Kabi AG

Luer-ended blood collection tube spike
Primary Device ID24086000101268
NIH Device Record Key4d533052-2935-497d-864e-32b9acb29f90
Commercial Distribution StatusIn Commercial Distribution
Brand NameMulti-Sampling Connector
Version Model Number4R5129
Catalog Number4R5129
Company DUNS315654579
Company NameFresenius Kabi AG
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Use once and destroy. Store at Room Temperature. Protect from freezing. Avoid excessive heat.

Device Identifiers

Device Issuing AgencyDevice ID
GS104086000101240 [Primary]
GS114086000101254 [Package]
Contains: 04086000101240
Package: Inner Pack [100 Units]
In Commercial Distribution
GS124086000101268 [Package]
Contains: 14086000101254
Package: Carton [20 Units]
In Commercial Distribution

FDA Product Code

KSTSystem, Blood Collection, Vacuum-Assisted, Manual

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-23
Device Publish Date2016-09-24

Devices Manufactured by Fresenius Kabi AG

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