Primary Device ID | 04049016109693 |
NIH Device Record Key | 81cc5be4-43e4-4c96-8419-75c6102f1056 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sprinter XL (model 160 samples, IFA incl. incubato |
Version Model Number | YG 0033-0101-4 |
Company DUNS | 322209263 |
Company Name | EUROIMMUN Medizinische Labordiagnostika AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04049016109693 [Primary] |
JQW | Station, Pipetting And Diluting, For Clinical Use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-24 |
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