| Primary Device ID | 00889024205116 |
| NIH Device Record Key | b3a055e7-d167-453f-bda5-3a954f7c9369 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AccuPort End Delivery Cannula 11 Ga x 120mm |
| Version Model Number | 307.034 |
| Catalog Number | 307.034 |
| Company DUNS | 078836317 |
| Company Name | ZIMMER KNEE CREATIONS, INC. |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Length | 120 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024205116 [Primary] |
| FGY | Cannula, Injection |
| MQV | Filler, Bone Void, Calcium Compound |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2016-05-18 |
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