FDA UDI In Commercial Distribution 🇺🇸 United States

AeroWrap™

DI: 00856525007280 · Model: Large · SUN SCIENTIFIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AeroWrap™
Primary DI
00856525007280
Version / Model
Large
Catalog Number
AW-LLB
Company Name
SUN SCIENTIFIC, INC.
Labeler DUNS
609397224
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-30
Public Version
2
Public Version Date
2022-06-23
Public Version Status
Update
Public Device Record Key
a2023ec3-3718-4227-ad89-8a38620b4ec4
Distribution End Date
2030-10-31

Device Description

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.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MHW Dressing, Compression

GMDN Terms

Code Name
16837 Sequential venous compression system

Identifiers

Type ID
Primary 00856525007280

Customer Contacts

Phone
9144795108

Premarket Submissions

Submission Number Supplement Number
K070457 000