| Primary Device ID | 30845854061095 |
| NIH Device Record Key | 353c802a-23ad-4faf-913f-88531cee4bca |
| Commercial Distribution Discontinuation | 2022-08-19 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | ALMA_KIT |
| Catalog Number | ALMA_KIT |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30845854061095 [Primary] |
| FYD | APPARATUS, EXHAUST, SURGICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-08-22 |
| Device Publish Date | 2020-06-18 |
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| 20653405990182 - CONMED | 2026-01-26 Universal Cart Strap |
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