AeroWrap™ AW-LMB,Short
GUDID 00856525007181
The AeroWrap ™ System is comprised of a gradient compression sleeve, and hand pump to provide static compression for compression therapy or DVT Prophylaxis. The AeroWrap™ gradient compression sleeve is a non-sterile single patient use medical device. The AeroWrap ™ Gradient Compression Sleeve contains a single bladder with a built-in gradient profile and inelastic straps to affix it to the patient’s leg. An inflation source is attached to the inflation valve on the sleeve. There is a inflation source provided: a hand pump to provide static compression. The system is intended for hospital and outpatient use.
SUN SCIENTIFIC, INC.
Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system Sequential venous compression system| Primary Device ID | 00856525007181 |
| NIH Device Record Key | 4c966957-0654-4090-ae26-aad95972da62 |
| Commercial Distribution Discontinuation | 2030-10-31 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AeroWrap™ |
| Version Model Number | Medium Short |
| Catalog Number | AW-LMB,Short |
| Company DUNS | 609397224 |
| Company Name | SUN SCIENTIFIC, 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 | false |
| 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
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00856525007181 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K070457
FDA Product Code
| JOW | Sleeve, Limb, Compressible |
| MHW | Dressing, Compression |
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 | 2021-05-10 |
| Device Publish Date | 2021-04-30 |
On-Brand Devices [AeroWrap™ ]
| 00856525007303 | The AeroWrap ™ System is comprised of a gradient compression sleeve, and hand pump to provide |
| 00856525007280 | The AeroWrap ™ System is comprised of a gradient compression sleeve, and hand pump to provide |
| 00856525007266 | The AeroWrap ™ System is comprised of a gradient compression sleeve, and hand pump to provide |
| 00856525007242 | The AeroWrap ™ System is comprised of a gradient compression sleeve, and hand pump to provide |
| 00856525007228 | The AeroWrap ™ System is comprised of a gradient compression sleeve, and hand pump to provide |
| 00856525007204 | The AeroWrap ™ System is comprised of a gradient compression sleeve, and hand pump to provide |
| 00856525007181 | The AeroWrap ™ System is comprised of a gradient compression sleeve, and hand pump to provide |
| 00856525007167 | The AeroWrap ™ System is comprised of a gradient compression sleeve, and hand pump to provide |
Trademark Results [AeroWrap]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 AEROWRAP 74078708 1694903 Dead/Cancelled |
FPM, INC. 1990-07-16 |
 AEROWRAP 73750051 1704856 Dead/Cancelled |
BXL PLASTICS LIMITED 1988-09-06 |
 AEROWRAP 73674182 1479604 Live/Registered |
SALEM LABEL COMPANY, INC. 1987-07-24 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.