FDA UDI In Commercial Distribution 🇺🇸 United States

Pak-Its™

DI: 00809958040621 · Model: 4839 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pak-Its™
Primary DI
00809958040621
Version / Model
4839
Catalog Number
DUP4839
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
3
Public Version Date
2022-12-20
Public Version Status
Update
Public Device Record Key
95fff23a-9e15-406e-b9f1-fc0921f99d3d

Device Description

0.5 in X 36 in surgical gauze packing. Non X-Ray detectable. Plain. 28 X 24 mesh gauze, cut edges. 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
48128 Gauze strip, non-antimicrobial

Identifiers

Type ID
Primary 00809958040621

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 0.5 in X 36 in