FDA UDI In Commercial Distribution 🇺🇸 United States

PrimaPad®

DI: 00809958087510 · Model: 83334 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
PrimaPad®
Primary DI
00809958087510
Version / Model
83334
Catalog Number
DUP83334
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
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
d1501f0c-ddb3-4540-a1c7-a6444ae78fc0

Device Description

3 in X 4 in non-adherent wound dressing. 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
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48134 Woven gauze pad

Identifiers

Type ID
Primary 00809958087510
Unit of Use 00809958087503

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 3 in X 4 in
Device Size Text, specify 7.5 cm X 10 cm