Primary Device ID | 07630030861482 |
NIH Device Record Key | 269742db-7e33-48d8-a2d9-096392128295 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | M.U.S.T. Anodized Rod |
Version Model Number | 03.55.802 |
Company DUNS | 488227125 |
Company Name | Medacta International SA |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07630030861482 [Primary] |
KWP | Appliance, Fixation, Spinal Interlaminal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-02-09 |
07630030877322 | Enhanced Anodized Rod Ti 5.5x480 |
07630030877315 | Enhanced Anodized Rod Ti 5.5x300 |
07630030877308 | Enhanced Anodized Rod Ti 5.5x200 |
07630030877292 | Enhanced Anodized Rod Ti 5.5x100 |
07630030877278 | Enhanced Anodized Rod Ti 5.5x480 - Unsterile |
07630030877261 | Enhanced Anodized Rod Ti 5.5x300 - Unsterile |
07630030877254 | Enhanced Anodized Rod Ti 5.5x200 - Unsterile |
07630030877247 | Enhanced Anodized Rod Ti 5.5x100 - Unsterile |
07630030861499 | Anodized Rod Ti 5.5x480 - Unsterile |
07630030861482 | Anodized Rod Ti 5.5x300 - Unsterile |
07630030861475 | Anodized Rod Ti 5.5x200 - Unsterile |
07630030861468 | Anodized Rod Ti 5.5x100 - Unsterile |
07630030861338 | Anodized Rod Ti 5.5x480 |
07630030861321 | Anodized Rod Ti 5.5x300 |
07630030861314 | Anodized Rod Ti 5.5x200 |
07630030861307 | Anodized Rod Ti 5.5x100 |