Primary Device ID | 05060418836511 |
NIH Device Record Key | f1a533eb-94ee-4fdf-a5f2-e98351d82306 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Susol® General Nipper Curved 13cm |
Version Model Number | SS08-0500-F |
Company DUNS | 769260357 |
Company Name | BAILEY INSTRUMENTS LTD |
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 | 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 | 05060418836504 [Package] Package: Pack [10 Units] In Commercial Distribution |
GS1 | 05060418836511 [Primary] |
JOK | Scissors, Medical, Disposable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-01-31 |
Device Publish Date | 2024-01-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SUSOL 78774087 3482237 Live/Registered |
LS Industrial Systems Co., Ltd. 2005-12-15 |