Primary Device ID | 00887482030110 |
NIH Device Record Key | 8be917a9-bd86-4650-ba94-aa9f4b57596e |
Commercial Distribution Discontinuation | 9999-01-01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Symmetry GIGLI |
Version Model Number | 75-1012 |
Catalog Number | 75-1012 |
Company DUNS | 079641356 |
Company Name | SYMMETRY SURGICAL 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 | 00887482030110 [Primary] |
GFA | Blade, Saw, General & Plastic Surgery, Surgical |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
Moist Heat or Steam Sterilization
[00887482030110]
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 | 2017-12-12 |
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