Primary Device ID | 00840606184601 |
NIH Device Record Key | 70f0d8da-4242-4afd-b740-d2e54ffdde51 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Magnum + |
Version Model Number | 15017-415 |
Company DUNS | 610712213 |
Company Name | SPINAL ELEMENTS, INC. |
Device Count | 1 |
DM Exempt | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840606184601 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
[00840606184601]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-02 |
Device Publish Date | 2024-04-24 |
00840606184632 | Magnum+ Punch Awl 20mm x 60° |
00840606184625 | Magnum+ Punch Awl 15mm x 60° |
00840606184618 | Magnum+ Punch Awl 20mm x 45° |
00840606184601 | Magnum+ Punch Awl 15mm x 45° |
00840606184588 | Magnum+ Punch Awl 20mm x Straight |
00840606184540 | Magnum+ Punch Awl 15mm x Straight |