FDA UDI In Commercial Distribution 🇺🇸 United States

DuPad®

DI: 00809958081716 · Model: 87059 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
DuPad®
Primary DI
00809958081716
Version / Model
87059
Catalog Number
DUP87059
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2018-10-23
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
a55c9808-4b6c-45a8-ba1e-7794b19524b6

Device Description

5 in X 9 in Closed end abdominal pad. 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
NAC Dressing, wound, hydrophilic

GMDN Terms

Code Name
48131 Non-woven gauze pad

Identifiers

Type ID
Primary 00809958081716
Unit of Use 00809958081709

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 12.7 cm X 22.9 cm
Device Size Text, specify 5 in X 9 in