| Primary Device ID | 20841019111141 |
| NIH Device Record Key | 7aee0428-0a58-471c-9f7c-8f5934d4d150 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Surgical West |
| Version Model Number | 10-4150SW |
| Company DUNS | 859400244 |
| Company Name | Surgical West, Inc. |
| 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 | false |
| 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 | 781-834-9500 |
| kprario@ksp.com |
| Length | 12 Feet |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841019111147 [Primary] |
| GS1 | 10841019111144 [Package] Contains: 00841019111147 Package: [10 Units] In Commercial Distribution |
| GS1 | 20841019111141 [Package] Contains: 00841019111147 Package: [50 Units] In Commercial Distribution |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20841019111141]
Radiation Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-10-27 |