| Primary Device ID | 00814334021903 |
| NIH Device Record Key | c2cbc141-db94-43cd-bb93-e872dde8ae2d |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 5161011 |
| Catalog Number | 5161011 |
| Company DUNS | 315304071 |
| Company Name | Richard Wolf GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| 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 | 00814334021903 [Primary] |
| NTN | Led light source |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-02-21 |
| Device Publish Date | 2017-07-21 |
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| 04055207069837 - NA | 2026-01-22 KERRISON SHEATH W 2MM WL 130MM 90° for use with Kerrison handle, reusable |
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