| Primary Device ID | 50628725005619 | 
| NIH Device Record Key | 8381cc32-e37c-42ba-b4d8-0469c1c35554 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Key Surgical | 
| Version Model Number | FL-2010 | 
| Catalog Number | FL-2010 | 
| Company DUNS | 240992693 | 
| Company Name | Canadian Hospital Specialties Limited | 
| 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 | true | 
| Serial Number | false | 
| Manufacturing Date | false | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | true | 
| RX Perscription | false | 
| OTC Over-The-Counter | false | 
| Phone | 9058259300 | 
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| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00628725005614 [Primary] | 
| GS1 | 50628725005619 [Package] Contains: 00628725005614 Package: case [20 Units] In Commercial Distribution | 
| NKC | Tubing/Tubing With Filter, Insufflation, Laparoscopic | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2020-12-11 | 
| Device Publish Date | 2020-12-03 | 
| 50628725005657 | Insufflation Tubing, ISO Connector | 
| 00628725005638 | Insufflation Tubing, Luer Connector | 
| 50628725005626 | Insufflation Tubing, Quick Connector | 
| 50628725005619 | Insufflation Tubing, Barb Connector | 
| 50628725005640 | Insufflation Tubing, Quick Connector | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  KEY SURGICAL  76691132  3671312 Live/Registered | KEY SURGICAL LLC 2008-07-09 |