RENASYS EDGE 66803126
GUDID 05000223498634
Renasys Edge Device
SMITH & NEPHEW MEDICAL LIMITED
Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable Negative-pressure wound therapy system, electric, reusable| Primary Device ID | 05000223498634 |
| NIH Device Record Key | 3fcfcbc8-1787-4b2b-a6fb-32f4bb0219ad |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RENASYS EDGE |
| Version Model Number | 66803126 |
| Catalog Number | 66803126 |
| Company DUNS | 216344051 |
| Company Name | SMITH & NEPHEW MEDICAL LIMITED |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Operating and Storage Conditions
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05000223498634 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K223041
FDA Product Code
| OMP | Negative Pressure Wound Therapy Powered Suction Pump |
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 | 2023-05-04 |
| Device Publish Date | 2023-04-26 |
On-Brand Devices [RENASYS EDGE]
| 05000223501549 | RENASYS EDGE Plug-in Mains Adapter Type A, CTN 1 |
| 05000223501150 | RENASYS EDGE Carry Straps |
| 05000223501136 | RENASYS EDGE Carry Bag |
| 05000223501105 | 800ml EDGE Canister without Solidifier |
| 05000223501082 | 800ml EDGE Canister with Solidifier |
| 05000223501068 | 300ml EDGE Canister without Solidifier |
| 05000223501044 | 300ml EDGE Canister with Solidifier |
| 05000223498634 | Renasys Edge Device |
Trademark Results [RENASYS EDGE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RENASYS EDGE 90845397 not registered Live/Pending |
T.J.Smith and Nephew,Limited 2021-07-23 |
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