Primary Device ID | 08806390859370 |
NIH Device Record Key | 030641d0-72da-40ca-9743-020f55063a0e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VERUM System Bone Screw |
Version Model Number | PR2518-L |
Company DUNS | 688811603 |
Company Name | Jeil Medical Corporation |
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 | 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 | 08806390859370 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08806390859370]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-11-11 |
Device Publish Date | 2017-10-25 |
08806390859554 | PR2530 |
08806390859547 | PR2528 |
08806390859530 | PR2526 |
08806390859523 | PR2524 |
08806390859516 | PR2522 |
08806390859509 | PR2520 |
08806390859493 | PR2518 |
08806390859486 | PR2516 |
08806390859479 | PR2514 |
08806390859462 | PR2512 |
08806390859455 | PR2510 |
08806390859448 | PR2508 |
08806390859431 | PR2530-L |
08806390859424 | PR2528-L |
08806390859417 | PR2526-L |
08806390859400 | PR2524-L |
08806390859394 | PR2522-L |
08806390859387 | PR2520-L |
08806390859370 | PR2518-L |
08806390859363 | PR2516-L |
08806390859356 | PR2514-L |
08806390859349 | PR2512-L |
08806390859332 | PR2510-L |
08806390859325 | PR2508-L |
08806390858038 | PH1506-L |
08806390858021 | CC0240 |
08806390858014 | CC0230 |