| Primary Device ID | EAMIAHK0070 |
| NIH Device Record Key | 34c09d6b-9291-4c64-a964-38ef37d351c2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | A.M.I. HAL Knotpusher |
| Version Model Number | AHK 007 |
| Catalog Number | AHK 007 |
| Company DUNS | 303655286 |
| Company Name | AMI Agency for Medical Innovations GmbH |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | EAMIAHK0070 [Primary] |
| HCF | Instrument, Ligature Passing And Knot Tying |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[EAMIAHK0070]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-12-31 |
| Device Publish Date | 2018-11-28 |
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