Primary Device ID | 00810021866550 |
NIH Device Record Key | bae5690c-b872-4776-8d77-7f013b81623c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CoLink LapiFix |
Version Model Number | C01 S4001 |
Catalog Number | C01 S4001 |
Company DUNS | 079700711 |
Company Name | IN2BONES USA, LLC |
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 |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810021866550 [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 | 2 |
Public Version Date | 2024-12-31 |
Device Publish Date | 2024-12-10 |
00810021866536 | CoLink LapiFix ASSEMBLY LEFT |
00810021866550 | CoLink LapiFix Disposable Instrument Set |