Primary Device ID | 08800039102216 |
NIH Device Record Key | 4e9d662c-4060-483a-9d19-2f446582713f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fixone Hybrid Anchor |
Version Model Number | KAPN-47501nc |
Company DUNS | 963422810 |
Company Name | AJU PHARM. CO., LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800039102216 [Primary] |
MAI | Fastener, Fixation, Biodegradable, Soft Tissue |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-01-14 |
Device Publish Date | 2025-01-06 |
08800039102254 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
08800039102216 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
08800039101035 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
08800039101028 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
08800039100601 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
08800039100571 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |