United States Endoscopy Group, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000017968 FEI 1000122656
- Devices
- 96
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
What United States Endoscopy Group, Inc. makes
United States Endoscopy Group, Inc. manufactures endoscopic accessories and procedural devices, including pull PEG kits, guidewire PEG kits, concentric balloon gastrostomy tools, disposable overtubes, coaxial and standard needles, papillotomes, electric biopsy forceps, balloon replacement gastrostomy tubes, and endoscopic retrieval devices. The portfolio also includes percutaneous endoscopic gastroscopy tools, color video cameras, and the AquaShield System for CO₂ management in endoscopic procedures.
The company’s devices are classified under Class II in the U.S. and are listed via FDA 510(k) clearance. The portfolio is regulated under U.S. medical device laws, and the manufacturer is based in the United States.
Catalogue
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Company details
- EUDAMED SRN
- US-MF-000017968
- FDA FEI number
- 1000122656
- EU VAT number
- 34-148202400
- EUDAMED status
- Active
- EUDAMED registered name
- United States Endoscopy Group, Inc.
- EUDAMED abbreviated name
- Also trading as US Endoscopy
- Registered address
- 5976, Heisley Rd, 44060, Mentor, Ohio, United States
- Website
- www.steris.com
- facebook.com/steriscorporate
- [email protected]
- Phone
- +353 (57) 860 6877
- PRRC contact
- Becky Aldhizer
From the company website
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention.