| Primary Device ID | 00887868134050 |
| NIH Device Record Key | ad9a9108-22f7-450a-bffc-5d6861a8a7c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 0.9MM K-WIRE DEPTH GAUGE |
| Version Model Number | 110018535 |
| Catalog Number | 110018535 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 | true |
| Serial Number | false |
| 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)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868134050 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868134050]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-01-21 |
| Device Publish Date | 2018-12-19 |
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| 00880304339224 - PARALLEL PULLER | 2024-09-11 |
| 00880304342187 - AGC MODULAR TIBIAL II | 2024-09-11 |
| 00880304365247 - BIO-MODULAR | 2024-09-11 |