FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617021140 · Model: 1121-36645 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617021140
Version / Model
1121-36645
Catalog Number
1121-36645
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-27
Public Version
4
Public Version Date
2023-12-06
Public Version Status
Update
Public Device Record Key
6a592c5b-33f9-4b4f-b519-ff3a6be76529

Device Description

Curaplex Fluff Bandage Roll, 4.5" x 147", 6 Ply, Non-sterile

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
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze/sponge,nonresorbable for external use

GMDN Terms

Code Name
48127 Woven gauze roll/sheet

Identifiers

Type ID
Package 00817617021157
Primary 00817617021140

Device Sizes

Type Value Unit Text
Weight 24 Gram