| Primary Device ID | 00628725005638 |
| NIH Device Record Key | 77936a94-75a0-4b45-b074-2ab0e6dd5680 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Key Surgical |
| Version Model Number | FL-2110 |
| Catalog Number | FL-2110 |
| 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 | 00628725005638 [Primary] |
| GS1 | 50628725005633 [Package] 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 |