| Primary Device ID | 04026575033690 |
| NIH Device Record Key | efcbaa25-7f43-4ea9-af47-32c78a9627d1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LINK Instruments - Chisel, bone curette, raspatory, rongeur |
| Version Model Number | 130-745 |
| Company DUNS | 315675488 |
| Company Name | WALDEMAR LINK GmbH & Co. KG |
| 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 | false |
| 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 |
|---|---|
| GS1 | 04026575033690 [Primary] |
| HTF | CURETTE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04026575033690]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-01-12 |
| Device Publish Date | 2023-01-04 |
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