Primary Device ID | 00888118106063 |
NIH Device Record Key | c50424a0-d399-4d4d-b86c-f0c05224f1c1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LEVEL ONE, STERILE |
Version Model Number | 24-015-67-71 |
Company DUNS | 826499238 |
Company Name | KLS-Martin L.P. |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00888118106063 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-03-09 |
Device Publish Date | 2018-09-27 |