| Primary Device ID | 10816207021116 | 
| NIH Device Record Key | 8c18903f-d5fe-4556-a46e-f02ceb1393e3 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | SwirlNet | 
| Version Model Number | ET2014 | 
| Catalog Number | ET2014 | 
| 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 | 
| 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 Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| Device Size Text, specify | 0 | 
| Length | 160 Centimeter | 
| Device Size Text, specify | 0 | 
| Outer Diameter | 3 Millimeter | 
| 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 Issuing Agency | Device ID | 
|---|---|
| GS1 | 00816207021119 [Primary] | 
| GS1 | 10816207021116 [Package] Contains: 00816207021119 Package: Box [5 Units] In Commercial Distribution | 
| FGX | Snare, Non-Electrical | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2022-09-29 | 
| Device Publish Date | 2022-09-21 | 
| 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 | 
| 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 |