Primary Device ID | 00841731106414 |
NIH Device Record Key | cfb077cc-6c4d-45e0-9aee-9f0f333749e5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cannulated Lesser Hemi Implant |
Version Model Number | MCHI-13 |
Company DUNS | 152008371 |
Company Name | VILEX IN TENNESSEE, INC. |
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 | 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 | 00841731106414 [Primary] |
KWD | Prosthesis, Toe, Hemi-, Phalangeal |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-04 |
00841731106414 | CHI, Mini 13_Ti Bronze |
00841731106407 | CHI, Mini 12_Ti Green |
00841731106391 | CHI, Mini 11_Ti Magenta |
00841731106384 | CHI, Mini 10_Ti Gold |
00841731106377 | CHI, Mini 09_Ti Blue |