SwirlNet ET2013
GUDID 10816207021109
Endoscopic Retrieval Net - Standard, Enteroscope
ENDO-THERAPEUTICS, INC.
Gastrointestinal/airway foreign body retrieval basket, single-use| Primary Device ID | 10816207021109 |
| NIH Device Record Key | 210b49f2-4227-4b69-952e-2ee29129a984 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SwirlNet |
| Version Model Number | ET2013 |
| Catalog Number | ET2013 |
| 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 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
| Device Size Text, specify | 0 |
| Length | 350 Centimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 2.5 Millimeter |
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 | 00816207021102 [Primary] |
| GS1 | 10816207021109 [Package] Contains: 00816207021102 Package: Box [5 Units] In Commercial Distribution |
FDA Product Code
| FGX | Snare, Non-Electrical |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
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 [SwirlNet]
| 10816207021123 | Endoscopic Retrieval Net - Maxi, Colonic |
| 10816207021116 | Endoscopic Retrieval Net - Maxi, Esophageal |
| 10816207021109 | Endoscopic Retrieval Net - Standard, Enteroscope |
| 10816207021093 | Endoscopic Retrieval Net - Standard, Colonic |
| 10816207021086 | Endoscopic Retrieval Net - Standard, Esophageal |
| 00816207021072 | Endoscopic Retrieval Net - Mini, Esophageal |
Trademark Results [SwirlNet]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SWIRLNET 87043082 5297482 Live/Registered |
Endo-Therapeutics, Inc. 2016-05-19 |
 SWIRLNET 77055631 3413933 Dead/Cancelled |
Swirlnet A/S 2006-12-01 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.