ENHANCE T903
GUDID 30845854052062
Enhance Allograft Wedge Instrumentation Tray
Conmed Corporation
Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable| Primary Device ID | 30845854052062 |
| NIH Device Record Key | 4ccc23ac-09d2-4423-8eba-a533e0eacc20 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ENHANCE |
| Version Model Number | T903 |
| Catalog Number | T903 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30845854052062 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K152969
FDA Product Code
| KCT | Sterilization wrap containers, trays, cassettes & other accessories |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
[30845854052062]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-05-06 |
| Device Publish Date | 2020-04-28 |
Devices Manufactured by Conmed Corporation
| 30845854080751 - PENADAPT | 2024-05-03 PenAdapt Electrosurgical Pencil Adapter 1 ft (30.5cm) tubing |
| 30845854061767 - NA | 2024-05-03 EY Tubing Kit 1-3/8 in (35mm) x 6 ft (1.8m) tube and six 2 ft (.6m) tubes with integral wand & sponge guard |
| 30845854045798 - CrossFT | 2024-04-26 CrossFT Knotless Biocomposite 4.0 mm Suture Anchor with one 2 mm Hi-Fi Tape (Blue) |
| 30845854650336 - CONMED | 2024-04-26 Lower Extremity Container, 3/4 Size, 6" Height |
| 30845854650343 - CONMED | 2024-04-26 Upper Extremity Container, 3/4 Size, 6" Height |
| 30845854026797 - GENESYS CrossFT, Hi-Fi | 2024-04-25 5.5 mm GENESYS CrossFT Suture Anchor with Three #2 (5 metric) Hi-Fi Sutures |
| 30845854026803 - GENESYS CrossFT, Hi-Fi | 2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Two #2 (5 metric) Hi-Fi Sutures |
| 30845854026810 - GENESYS CrossFT, Hi-Fi | 2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Three #2 (5 metric) Hi-Fi Sutures |
Trademark Results [ENHANCE]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.