FDA UDI In Commercial Distribution 🇺🇸 United States

Derma

DI: 00809958000991 · Model: 3473 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Basic Information

Brand Name
Derma
Primary DI
00809958000991
Version / Model
3473
Catalog Number
DUP3473
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2018-10-23
Public Version
3
Public Version Date
2023-02-20
Public Version Status
Update
Public Device Record Key
5e2259c0-84e7-4944-8996-76ecae4836b1

Device Description

1 lb absorbent cotton roll

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
No
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
58232 Cotton wool roll

Identifiers

Type ID
Primary 00809958000991
Unit of Use 00809958000601

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 0.45 kg
Device Size Text, specify 1 lb