| Primary Device ID | 30845854061439 |
| NIH Device Record Key | ba6e73e6-7632-409d-aad8-462ad313cea6 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 57525685 |
| Catalog Number | 57525685 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| 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 | 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 | 00845854061438 [Unit of Use] |
| GS1 | 30845854061439 [Primary] |
| GAZ | TUBING, NONINVASIVE |
| KDQ | BOTTLE, COLLECTION, VACUUM |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-08-14 |
| Device Publish Date | 2020-08-06 |
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