FDA UDI In Commercial Distribution 🇺🇸 United States

GoodSense

DI: 00180410000880 · Model: 180410000880 · GEISS, DESTIN & DUNN, INC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
GoodSense
Primary DI
00180410000880
Version / Model
180410000880
Company Name
GEISS, DESTIN & DUNN, INC
Labeler DUNS
076059836
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2020-08-28
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
ff225e37-8fe7-4e4d-b6bf-b70a08bd1a03

Device Description

Sterile Pads, all one size, 3 IN x 3 IN (76 mm x 76 mm)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
48131 Non-woven gauze pad

Identifiers

Type ID
Package 10180410000887
Primary 00180410000880
Unit of Use 60180410000882

Customer Contacts

Phone
8558234545