| Primary Device ID | 30653405988292 | 
| NIH Device Record Key | 263e202c-a9bc-4672-a86d-975787bc5bc5 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Version Model Number | IFS-FUSE | 
| Catalog Number | IFS-FUSE | 
| 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 | 
| 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 | 30653405988292 [Primary] | 
| HIF | Insufflator, laparoscopic | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2022-06-10 | 
| Device Publish Date | 2022-06-02 | 
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