FDA UDI In Commercial Distribution 🇺🇸 United States

DuLap®

DI: 00809958013304 · Model: 1293 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DuLap®
Primary DI
00809958013304
Version / Model
1293
Catalog Number
DUP1293
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-13
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
bd51cf91-cd6b-4ba9-a37c-9f3ec4f3eebc

Device Description

18 in X 36 in 4 ply Laparotomy Songes, Prewashed, Folded, Wrapped.

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 00809958013304

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 18 in X 36 in
Device Size Text, specify 46 cm X 91 cm