| Primary Device ID | 08717903495407 |
| NIH Device Record Key | c6567608-7927-4b23-bd20-6b901235bbc7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Humeca blade for Aesculap®/Acculan® dermatome |
| Version Model Number | 5.BL4245/1 |
| Catalog Number | 5.BL4245/1 |
| Company DUNS | 489831498 |
| Company Name | Humeca B.V. |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08717903490198 [Primary] |
| GS1 | 08717903495407 [Package] Contains: 08717903490198 Package: Box [10 Units] In Commercial Distribution |
| GFD | Dermatome |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-28 |
| Device Publish Date | 2025-05-20 |
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| 08717903495407 - Humeca blade for Aesculap®/Acculan® dermatome | 2025-05-28 |
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