Primary Device ID | 04050588000073 |
NIH Device Record Key | af71e66c-d359-41e3-87eb-1a7af63becb2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | mercury® lt med |
Version Model Number | cos30000va07 |
Catalog Number | cos30000va07 |
Company DUNS | 341362614 |
Company Name | h/p/cosmos sports & medical gmbh |
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 | 04050588000073 [Primary] |
IOL | Treadmill, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-05-19 |
Device Publish Date | 2020-01-07 |
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04050588000073 - mercury® lt med | 2020-05-19 |
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04050588000516 - quasar® lt med | 2020-05-19 |