Primary Device ID | 00859464007212 |
NIH Device Record Key | c6f05bb9-2fb0-4305-ac33-0fac86e3337b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Turbett Surgical |
Version Model Number | TS1000 |
Company DUNS | 080273036 |
Company Name | Turbett Surgical Inc |
Device Count | 1 |
DM Exempt | true |
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 | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00859464007212 [Primary] |
FRG | Wrap, Sterilization |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-18 |
Device Publish Date | 2023-07-10 |
00859464007281 | Turbett Surgical TS1200 Container |
00859464007212 | Turbett Surgical TS1000 containers |
00859464007113 | TS1500 Container |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TURBETT SURGICAL 97543334 not registered Live/Pending |
Turbett Surgical, Inc. 2022-08-10 |
TURBETT SURGICAL 87145790 5273007 Live/Registered |
Turbett Surgical LLC 2016-08-22 |