| Primary Device ID | B3901884024T1 |
| NIH Device Record Key | 8daafbea-d8c5-474d-a8e3-3cc7179cdd9b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Reprocessed 4mm Skimmer Angle Tip Blade, 27.5cm |
| Version Model Number | 18-84024T |
| Company DUNS | 785616934 |
| Company Name | SURETEK MEDICAL |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B3901884024T1 [Primary] |
| NBH | Accessories, Arthroscopic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-07-04 |
| Device Publish Date | 2019-05-15 |
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