Primary Device ID | 03700712401078 |
NIH Device Record Key | 5e5d92f7-5f46-4e2c-8522-5f486f53566a |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | ARD515031880A |
Company DUNS | 264700139 |
Company Name | MAQUET SAS |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | 03700712401078 [Primary] |
FSY | Light, surgical, ceiling mounted |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-01-08 |
Device Publish Date | 2016-09-12 |
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