FDA UDI In Commercial Distribution 🇺🇸 United States

Co-Ease

DI: 00857425005833 · Model: CE20LFS · Hemasource, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Co-Ease
Primary DI
00857425005833
Version / Model
CE20LFS
Company Name
Hemasource, Inc.
Labeler DUNS
009046405
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
080733df-50d6-44f2-ace7-154ce88f002c

Device Description

Co-Ease 2" x 5 yds. Sterile. LF. TAN

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FQM Bandage, Elastic

GMDN Terms

Code Name
58964 Non-adhesive device retention bandage

Identifiers

Type ID
Package 10857425005830
Primary 00857425005833
Package 20857425005837