Primary Device ID | 00880304376014 |
NIH Device Record Key | d3f4e7b5-7506-4856-adbe-a013f41fc563 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TREPHINE SLAP-HAMMER |
Version Model Number | 430105 |
Catalog Number | 430105 |
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 | 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 |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304376014 [Primary] |
FZY | HAMMER, SURGICAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304376014]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-07-28 |
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00880304342187 - AGC MODULAR TIBIAL II | 2024-09-11 |
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00880304368637 - BOHN MODULAR FEMORAL STEM EXTRACTOR | 2024-09-11 |