FDA UDI In Commercial Distribution 🇺🇸 United States

COLOPLAST PREP

DI: 00311701007039 · Model: 0925 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
COLOPLAST PREP
Primary DI
00311701007039
Version / Model
0925
Catalog Number
0925
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-22
Public Version
3
Public Version Date
2023-02-20
Public Version Status
Update
Public Device Record Key
ec2bdafa-c674-48d3-9e1f-50d898a07f54

Device Description

Skin Barrier Wipe

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
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NEC Bandage, liquid, skin protectant

GMDN Terms

Code Name
58978 Synthetic-polymer liquid barrier dressing

Identifiers

Type ID
Package 00311701007930
Primary 00311701007039

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 2 Fluid Ounce