ACE-FISCHER®PIN HOLDER BOLT 100163
GUDID 00887868003059
Biomet Orthopedics, LLC
External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use| Primary Device ID | 00887868003059 |
| NIH Device Record Key | a22b318e-62ff-47e9-9a5e-7180a3a3da6b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ACE-FISCHER®PIN HOLDER BOLT |
| Version Model Number | 10016-3 |
| Catalog Number | 100163 |
| 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 | true |
| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868003059 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
FDA Product Code
| HXK | HOLDER, NEEDLE; ORTHOPEDIC |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
[00887868003059]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
Devices Manufactured by Biomet Orthopedics, LLC
| 00887868004087 - PRIMARY TREPHINE | 2024-04-03 |
| 00887868004094 - BUSHING | 2024-04-03 |
| 00887868004100 - SECONDARY TREPHINE | 2024-04-03 |
| 00887868048272 - TREPHINE | 2024-04-03 |
| 00887868048289 - TREPHINE | 2024-04-03 |
| 00887868048296 - TREPHINE | 2024-04-03 |
| 00887868048302 - TREPHINE | 2024-04-03 |
| 00880304658387 - Compress® | 2024-03-11 |
Trademark Results [ACE-FISCHER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ACE-FISCHER 73421065 1281428 Live/Registered |
Ace Orthopedic Company, Inc. 1983-04-11 |
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