eSuction ET2000
GUDID 10816207020966
Foreign Body Retrieval, Esophageal
ENDO-THERAPEUTICS, INC.
Gastrointestinal/airway foreign body retrieval basket, single-use| Primary Device ID | 10816207020966 |
| NIH Device Record Key | f8e33b1b-3894-4b17-bbbb-5003ad197f4f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | eSuction |
| Version Model Number | ET2000 |
| Catalog Number | ET2000 |
| Company DUNS | 825239189 |
| Company Name | ENDO-THERAPEUTICS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com | |
| Phone | 844-400-3636 |
| customerservice@endotherapeutics.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 19 Millimeter |
| Device Size Text, specify | 0 |
| Length | 230 Centimeter |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816207020969 [Primary] |
| GS1 | 10816207020966 [Package] Contains: 00816207020969 Package: Box [3 Units] In Commercial Distribution |
FDA Product Code
| FGX | Snare, Non-Electrical |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-29 |
| Device Publish Date | 2022-09-21 |
On-Brand Devices [eSuction]
| 10816207020973 | Foreign Body Retrieval, Colonic |
| 10816207020966 | Foreign Body Retrieval, Esophageal |
Trademark Results [eSuction]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ESUCTION 87041855 5229374 Live/Registered |
Endo-Therapeutics, Inc. 2016-05-18 |
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