FDA UDI In Commercial Distribution 🇺🇸 United States

DuForm®

DI: 00809958073902 · Model: 75206 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DuForm®
Primary DI
00809958073902
Version / Model
75206
Catalog Number
DUP75206
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-13
Public Version
3
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
874687d7-499b-4f72-bbbc-0e42252be651

Device Description

6 in X 4.1 yards stretched, sterile conforming bandage.

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
48127 Woven gauze roll/sheet

Identifiers

Type ID
Primary 00809958073902

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 15 cm X 3.7 cm
Device Size Text, specify 6 in X 4.1 yards