| Primary Device ID | 00889024704008 |
| NIH Device Record Key | a9ee5f42-9dea-4e59-a3fe-ce96e695d6ea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LB Type 1 Taper Extraction Insert |
| Version Model Number | SSI008216 |
| Catalog Number | SSI008216 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | false |
| 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 |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024704008 [Primary] |
| HWB | Extractor |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024704008]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-26 |
| Device Publish Date | 2025-12-18 |
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