Primary Device ID | 08426950870227 |
NIH Device Record Key | d143acfd-3198-46f1-aadf-a69f9bce2e11 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GEM Premier 5000 |
Version Model Number | 00024019255 |
Catalog Number | 00024019255 |
Company DUNS | 557223252 |
Company Name | INSTRUMENTATION LABORATORY COMPANY |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08426950870227 [Primary] |
CHL | Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-07-12 |
Device Publish Date | 2017-03-29 |
00195226000528 - ACL TOP 770 | 2024-05-23 ACL TOP 770 |
00195226000535 - ACL TOP 770 LAS | 2024-05-23 ACL TOP 770 LAS |
00195226000542 - ACL TOP 770s | 2024-05-23 ACL TOP 770s |
00195226000559 - ACL TOP 570 | 2024-05-23 ACL TOP 570 |
00195226000566 - ACL TOP 370 | 2024-05-23 ACL TOP 370 |
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