FDA UDI In Commercial Distribution 🇺🇸 United States

Dupress®

DI: 00809958183014 · Model: 89403 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
60

Basic Information

Brand Name
Dupress®
Primary DI
00809958183014
Version / Model
89403
Catalog Number
DUP89403
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
60
Record Status
Published
Publish Date
2018-10-23
Public Version
1
Public Version Date
2018-11-23
Public Version Status
New
Public Device Record Key
1f3edcca-7d61-44c0-88f2-74ebbf13f9ce

Device Description

4 in X 4 in Pressure bandage composed of conforming bandage and non-adherent pad. Medium. Sterile

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FQM BANDAGE, ELASTIC

GMDN Terms

Code Name
34864 Adhesive bandage

Identifiers

Type ID
Primary 00809958183014
Unit of Use 00809958183007

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 10 cm X 10 cm
Device Size Text, specify 4 in X 4 in