Primary Device ID | 00880304568402 |
NIH Device Record Key | 3053a942-47f2-4b87-8d07-77c128f7e3e5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PRECISION NITINOL GUIDE WIRE |
Version Model Number | 110008343 |
Catalog Number | 110008343 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304568402 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-09-18 |
Device Publish Date | 2020-05-23 |
00880304568532 | 110009769 |
00880304568402 | 110008343 |