| Primary Device ID | 00889024583337 |
| NIH Device Record Key | 255469a9-5846-4189-ae4d-feafffc772e6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 1mm PPK Resection Shim |
| Version Model Number | SSI005422 |
| Catalog Number | SSI005422 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 | 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 | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024583337 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
[00889024583337]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-02-11 |
| Device Publish Date | 2020-02-03 |
| 00887868571718 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571725 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571732 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571749 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571756 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571763 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571770 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571787 - RingLoc®+ Triflange | 2025-06-20 |