eSuction ET2001
Ref ET2001
eSuction ET2001 is a Class I device made by Endo-Therapeutics Inc., registered in EUDAMED on 26 May 2026 (Basic UDI-DI B-00816207020976) and listed in FDA GUDID since 21 Sep 2022 (UDI-DI 00816207020976), active as of 8 Nov 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-00816207020976 00816207020976 | Date26 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00816207020976 | Date21 Sep 2022 | StatusListed |
Official records
- EUDAMED public site B-00816207020976
- AccessGUDID record 00816207020976
Across registries
- EUDAMED Basic UDI-DI B-00816207020976 registered 26 May 2026 Active
- FDA GUDID UDI-DI 00816207020976 listed 21 Sep 2022 Listed
Timeline
- Listed FDA GUDID 00816207020976
- Registered EUDAMED B-00816207020976
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- eSuction
- Generic name
- Gastrointestinal/airway foreign body retrieval basket, single-use
- Device name
- Foreign Body Retrieval
- Model / Ref / Catalog
- ET2001
- Primary DI / UDI-DI
- 00816207020976
- Basic UDI-DI
- B-00816207020976
- FDA product code
- FGX
- EMDN code
- G03050199 Digestive endoscopy, retrieval devices - other
- GMDN term
- Gastrointestinal/airway foreign body retrieval basket, single-use
- Device class
- Class I
- Regulation number
- 876.4730
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Malta
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 19 MillimeterLength — 230 Centimeter
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