FDA Registration Active 🇺🇸 United States

Sheridan Spiral-Flex Reinforced Endotracheal Tube

Reg #: 3004111573 · FEI: 3004111573 · Expires 2025
Products
1
Proprietary Names
19
Establishment Types
1
Classifications
1

Registration Details

Registration Name
Sterigenics US LLC
Registration Number
3004111573
FEI Number
3004111573
Status
Active
Expiry Year
2025
Initial Importer
No
Address
1302 Avenue T
City
Grand Prairie
State
TX
ZIP
75050
Country
US

Regulatory Submissions

510(k) Number
K844296

Owner / Operator

Firm Name
Sotera Health LLC
Operator Number
10029425
Address
2015 Spring Road, Suite 650
City
Oak Brook
State
IL
Postal Code
60523
Country
US
Correspondent
Karen Whaley-Krumins

Products

Device Name Product Code
Tube, Tracheal (W/Wo Connector) BTR

Proprietary Names

Sheridan Spiral-Flex Reinforced Endotracheal Tube ET TUBE CUFFED SPIRAL-FLEX 9 ET TUBECUFFED ORALSPIRAL-FLEX 5.5 ET TUBECUFFED ORALSPIRAL-FLEX 6.5 ET TUBECUFFED ORALSPIRAL-FLEX 9 ET TUBE CUFFED SPIRAL-FLEX 7 ET TUBE CUFFED SPIRAL-FLEX 8.5 ET TUBE CUFFED SPIRAL-FLEX 6 ET TUBECUFFED ORALSPIRAL-FLEX 7 ET TUBECUFFED ORALSPIRAL-FLEX 8.5 ET TUBECUFFED ORALSPIRAL-FLEX 7.5 ET TUBECUFFED ORALSPIRAL-FLEX 8 ET TUBE CUFFED SPIRAL-FLEX 6.5 ET TUBECUFFED ORALSPIRAL-FLEX 6 ET TUBE CUFFED SPIRAL-FLEX 5.5 ET TUBECUFFED ORALSPIRAL-FLEX 5 ET TUBE CUFFED SPIRAL-FLEX 5 ET TUBE CUFFED SPIRAL-FLEX 7.5 ET TUBE CUFFED SPIRAL-FLEX 8

Establishment Types

Sterilize Medical Device for Another Party (Contract Sterilizer)