FDA UDI In Commercial Distribution 🇺🇸 United States

DuLap®

DI: 00809958010822 · Model: 1206 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
60

Basic Information

Brand Name
DuLap®
Primary DI
00809958010822
Version / Model
1206
Catalog Number
DUP1206
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
60
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
cf57bbd8-d059-4cdb-9ff8-a2b4924cb4a2

Device Description

12 in X 12 in 4 ply Laparotomy Sponges. Prewashed

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
GDY GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE

GMDN Terms

Code Name
38496 Radiopaque woven surgical sponge

Identifiers

Type ID
Primary 00809958010822
Unit of Use 00809958010808

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 30 cm X 30 cm
Device Size Text, specify 12 in X 12 in