FDA UDI In Commercial Distribution 🇺🇸 United States

Suprathel®

DI: 04260184021437 · Model: Suprathel 18x23 · Polymedics Innovations GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Suprathel®
Primary DI
04260184021437
Version / Model
Suprathel 18x23
Catalog Number
111823-US, 151823-US
Company Name
Polymedics Innovations GmbH
Labeler DUNS
344089540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-17
Public Version
1
Public Version Date
2021-09-27
Public Version Status
New
Public Device Record Key
bcb0a24c-3c86-4b28-ba65-8a1d1d46802b

Device Description

Suprathel® is an absorbable, microporous membrane and alloplastic skin substitute for the treatment of wounds, split-skin donor sites, and burns as indicated hereinafter. The device is supplied sterile in a variety of sizes to be trimmed by the surgeon to meet the individual patient’s needs.

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
FRO Dressing, Wound, Drug

GMDN Terms

Code Name
64853 Synthetic wound matrix dressing

Identifiers

Type ID
Package 04260184021475
Primary 04260184021437
Package 04260184021482

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K090160 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
8 – 22 Degrees Celsius