| Primary Device ID | 05060423410119 |
| NIH Device Record Key | 966c31e9-e8d4-4a7a-81af-cfb08969d5b8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Endocuff |
| Version Model Number | AEC140 |
| Company DUNS | 216745893 |
| Company Name | BODDINGTONS PLASTICS LIMITED |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Lumen/Inner Diameter | 12.1 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05060423410119 [Primary] |
| GS1 | 5060423410034 [Package] Package: Carton [8 Units] In Commercial Distribution |
| GS1 | 5060423410157 [Package] Contains: 5060423410034 Package: Shipper [120 Units] In Commercial Distribution |
| FED | Endoscopic Access Overtube, Gastroenterology-Urology |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-08 |
| 05060423410119 | AEC140 Size 4 (Xl) Endocuff Sterile Orange- 1 pot - single unit |
| 05060423410102 | AEC130 Size 3 (S) Endocuff Sterile Purple- 1 pot - single unit |
| 05060423410096 | AEC120 Size 2 (L) Endocuff Sterile Green- 1 pot - single unit |
| 05060423410089 | AEC110 Size 1 (M) Endocuff Sterile Blue - 1 pot - single unit |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ENDOCUFF 79120509 4492954 Live/Registered |
ARC Medical Design Limited 2012-09-07 |
![]() ENDOCUFF 76220865 not registered Dead/Abandoned |
Advanced Surgical Concepts Limited 2001-03-05 |