FDA UDI In Commercial Distribution 🇺🇸 United States

Suprathel® CW

DI: 04260184022236 · Model: Suprathel CW 9x10 · Polymedics Innovations GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Suprathel® CW
Primary DI
04260184022236
Version / Model
Suprathel CW 9x10
Catalog Number
210910-US, 250910-US
Company Name
Polymedics Innovations GmbH
Labeler DUNS
344089540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-11
Public Version
1
Public Version Date
2024-10-21
Public Version Status
New
Public Device Record Key
133edf02-0bef-4158-9bec-c72bceb906cc

Device Description

Suprathel® CW is an absorbable, micro-porous membrane and alloplastic skin substitute for the treatment of wounds, including pressure and venous ulcers, venous stasis and diabetic ulcers, ulcers caused by mixed vascular etiologies.

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
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QSZ Absorbable Synthetic Wound Dressing

GMDN Terms

Code Name
64853 Synthetic wound matrix dressing

Identifiers

Type ID
Package 04260184022281
Primary 04260184022236
Package 04260184022298

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K090160 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 22 Degrees Celsius