FDA UDI In Commercial Distribution 🇺🇸 United States

Aero-Wrap™ Bilateral Kit, Extra Large

DI: 00856525007556 · Model: AW6580-03 · SUN SCIENTIFIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aero-Wrap™ Bilateral Kit, Extra Large
Primary DI
00856525007556
Version / Model
AW6580-03
Catalog Number
AWB-LLBX
Company Name
SUN SCIENTIFIC, INC.
Labeler DUNS
609397224
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-29
Public Version
2
Public Version Date
2022-06-23
Public Version Status
Update
Public Device Record Key
8186edc1-5436-4005-9c8b-f31be50da31b
Distribution End Date
2030-10-31

Device Description

The AeroWrap ™ Bilateral Kit System is comprised of two gradient compression sleeves, and a hand pump to provide static compression for compression therapy or DVT Prophylaxis. The AeroWrap™ kit system gradient compression sleeves are non-sterile single patient use medical device. The AeroWrap™ Bilateral Kit Gradient Compression Sleeves contains a single bladder with a built-in gradient profile and inelastic straps to affix it to the patient’s legs from the ankle to the knee. 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)
Yes
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 00856525007556

Customer Contacts

Phone
9144795108

Premarket Submissions

Submission Number Supplement Number
K070457 000