FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617021126 · Model: 1121-36545 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617021126
Version / Model
1121-36545
Catalog Number
1121-36545
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
5
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
9ae79471-cc4a-4f98-9796-3edcff3958d3

Device Description

Curaplex Fluff Bandage Roll, 4.5" x 147", 6 Ply, 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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
NAB Gauze/sponge,nonresorbable for external use

GMDN Terms

Code Name
48127 Woven gauze roll/sheet

Identifiers

Type ID
Package 00817617021133
Primary 00817617021126

Device Sizes

Type Value Unit Text
Weight 24 Gram