FDA UDI In Commercial Distribution 🇺🇸 United States

Derma

DI: 00809958000281 · Model: 9002 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Derma
Primary DI
00809958000281
Version / Model
9002
Catalog Number
DUP9002
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2018-10-23
Public Version
3
Public Version Date
2022-12-20
Public Version Status
Update
Public Device Record Key
3b3c69ed-5b18-43d8-bf04-d4fa55303697

Device Description

0.50 in X 100 yards, non X-Ray detectable surgical gauze packing, made from 28 X 24 mesh gauze, 4-Ply.

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
48128 Gauze strip, non-antimicrobial

Identifiers

Type ID
Primary 00809958000281
Unit of Use 00809958000663

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 0.5 in X 100 yards
Device Size Text, specify 1.27 cm X 91.4 m