Primary Device ID | 00816611023709 |
NIH Device Record Key | 8faadf7d-6372-48be-b207-848ffba94d63 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AngioSystems Tray |
Version Model Number | 5680-4 |
Company DUNS | 144884467 |
Company Name | ANGIOSYSTEMS, INCORPORATED |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 00816611023693 [Primary] |
GS1 | 00816611023709 [Package] Contains: 00816611023693 Package: [30 Units] In Commercial Distribution |
LRP | Tray, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-01 |
Device Publish Date | 2018-08-29 |
00816611025147 | KM5067 |
00816611025123 | KM5066 |
00816611025062 | KM5065 |
00816611025048 | KM5064 |
00816611024782 | 43545-3 |
00816611024768 | 1056 |
00816611024744 | 1055 |
00816611024720 | 1036 |
00816611024706 | 1015 |
00816611024683 | 1002-2 |
00816611024669 | 1000 |
00816611024645 | KM5063 |
00816611024621 | KM5062 |
00816611024607 | KM5061 |
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00816611024546 | KM5057 |
00816611024522 | KM5056 |
00816611024508 | KM5055 |
00816611024485 | KM5054 |
00816611024461 | KM5052 |
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00816611024089 | KM5017 |
00816611024065 | KM5014 |
00816611024041 | KM5009 |
00816611024027 | 5680-11 |
00816611024003 | 5125 |
00816611023983 | 5120 |
00816611023969 | 5800 |
00816611023945 | 5744 |
00816611023921 | 5743 |
00816611023907 | 5742 |
00816611023884 | 5732 |