FDA Registration Active 🇧🇪 Belgium

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl

Reg #: 3005941719 · FEI: 3002807111 · Expires 2025
Products
1
Proprietary Names
10
Establishment Types
1
Classifications
1

Registration Details

Registration Name
Sterigenics Belgium Petit Rechain S.A.
Registration Number
3005941719
FEI Number
3002807111
Status
Active
Expiry Year
2025
Initial Importer
No
Address
Zoning Industriel de Petit-Rechain, Avenue Andre Ernst 21
City
Verviers Liege
Country
BE

Regulatory Submissions

510(k) Number
K041348

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 Tracheostomy And Tube Cuff JOH

Proprietary Names

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 8MM BLU TUBE +2/CA Portex UltraPerc Sing ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 9MM BLU TUBE +2/CA Portex UltraPerc Sing ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLUS TUBE +2/CA Portex UltraPerc Sin ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 9MM BLUS TUBE +2/CA Portex UltraPerc Sin ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 8MM BLUS TUBE +2/CA Portex UltraPerc Sin Portex Ultraperc K041348 ULTRAPERC PERC S/S DILATION TRACHY KIT FOR 7, 8, 9MM TUBES, SOFT INTRODUCERS, 2/CA Portex UltraPerc Percutaneous T ULTRAPERC LOCAL INFILTRATION (SDD) W/DRUGS + 10/CA Portex UltraPerc Local Infiltration Tray

Establishment Types

Sterilize Medical Device for Another Party (Contract Sterilizer)