SPINE SYSTEM 1200-1212
GUDID 00888480141792
BIOMET SPINE LLC
Bone-screw internal spinal fixation system, non-sterile| Primary Device ID | 00888480141792 |
| NIH Device Record Key | a77677d6-4f99-4ae2-8069-a1e20563208d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SPINE SYSTEM |
| Version Model Number | 1200-1212 |
| Catalog Number | 1200-1212 |
| Company DUNS | 018577570 |
| Company Name | BIOMET SPINE 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 Dimensions
| 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 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00888480141792 [Primary] |
FDA Product Code
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
[00888480141792]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-10-27 |
On-Brand Devices [SPINE SYSTEM]
Trademark Results [SPINE SYSTEM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SPINE SYSTEM 74164936 1732796 Live/Registered |
AESCULAP AG. 1991-05-09 |
 SPINE SYSTEM 74164935 1864032 Live/Registered |
AESCULAP AG. 1991-05-09 |
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