Primary Device ID | 00852588007090 |
NIH Device Record Key | 0b37709e-7740-44de-9b3f-83aac8d739e6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INSUFLOW SYNERGY XL PORT |
Version Model Number | 1991-8 |
Catalog Number | 1991-8 |
Company DUNS | 848693730 |
Company Name | LEXION MEDICAL, LLC |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852588007090 [Primary] |
HIF | Insufflator, Laparoscopic |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
[00852588007090]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-01-09 |
Device Publish Date | 2017-02-15 |
00852588007144 | 12mm X 130mm GAS CONDITIONING PORT |
00852588007137 | 10mm X 130mm GAS CONDITIONING PORT |
00852588007120 | 8mm X 130mm GAS CONDITIONING PORT |
00852588007113 | 12mm GAS CONDITIONING PORT |
00852588007106 | 10mm GAS CONDITIONING PORT |
00852588007090 | 8mm GAS CONDITIONING PORT |